G CEP120 | |||
Description: centrosomal protein 120 Associations 174 Studies 158 |
V rs2115172 | |||
Location: 5:123349434 Cytogenetic region:5q23.2 Most severe consequence: Intron variant Mapped gene(s): CEP120 Associations 1 Studies 1 |
V rs10051787 | |||
Location: 5:123396542 Cytogenetic region:5q23.2 Most severe consequence: Intron variant Mapped gene(s): CEP120 Associations 3 Studies 1 |
V rs17473412 | |||
Location: 5:123361737 Cytogenetic region:5q23.2 Most severe consequence: Intron variant Mapped gene(s): CEP120 Associations 1 Studies 1 |
V rs6595440 | |||
Location: 5:123383042 Cytogenetic region:5q23.2 Most severe consequence: Missense variant Mapped gene(s): CEP120 Associations 2 Studies 2 |
V rs1864046 | |||
Location: 5:123405227 Cytogenetic region:5q23.2 Most severe consequence: Intron variant Mapped gene(s): CEP120 Associations 1 Studies 1 |
V rs6595443 | |||
Location: 5:123407631 Cytogenetic region:5q23.2 Most severe consequence: Intron variant Mapped gene(s): CEP120 Associations 1 Studies 1 |
V rs7706662 | |||
Location: 5:123419868 Cytogenetic region:5q23.2 Most severe consequence: Intron variant Mapped gene(s): CEP120 Associations 2 Studies 2 |
V rs6862676 | |||
Location: 5:123408311 Cytogenetic region:5q23.2 Most severe consequence: Intron variant Mapped gene(s): CEP120 Associations 3 Studies 1 |
V rs28891214 | |||
Location: 5:123355195 Cytogenetic region:5q23.2 Most severe consequence: Intron variant Mapped gene(s): CEP120 Associations 2 Studies 2 |
V rs9327294 | |||
Location: 5:123381125 Cytogenetic region:5q23.2 Most severe consequence: Intron variant Mapped gene(s): CEP120 Associations 3 Studies 3 |
V rs11241692 | |||
Location: 5:123392125 Cytogenetic region:5q23.2 Most severe consequence: Intron variant Mapped gene(s): CEP120 Associations 1 Studies 1 |
V rs17474406 | |||
Location: 5:123396648 Cytogenetic region:5q23.2 Most severe consequence: Intron variant Mapped gene(s): CEP120 Associations 1 Studies 1 |
V rs34732995 | |||
Location: 5:123363505 Cytogenetic region:5q23.2 Most severe consequence: Intron variant Mapped gene(s): CEP120 Associations 9 Studies 9 |
V rs2303720 | |||
Location: 5:123346640 Cytogenetic region:5q23.2 Most severe consequence: Missense variant Mapped gene(s): CEP120 Associations 2 Studies 2 |
V rs6595447 | |||
Location: 5:123415153 Cytogenetic region:5q23.2 Most severe consequence: Intron variant Mapped gene(s): CEP120 Associations 2 Studies 2 |
V rs11948639 | |||
Location: 5:123406052 Cytogenetic region:5q23.2 Most severe consequence: Intron variant Mapped gene(s): CEP120 Associations 1 Studies 1 |
V rs34768912 | |||
Location: 5:123417297 Cytogenetic region:5q23.2 Most severe consequence: Intron variant Mapped gene(s): CEP120 Associations 1 Studies 1 |
V rs1428388 | |||
Location: 5:123368955 Cytogenetic region:5q23.2 Most severe consequence: Intron variant Mapped gene(s): CEP120 Associations 1 Studies 1 |
V rs9327293 | |||
Location: 5:123363731 Cytogenetic region:5q23.2 Most severe consequence: Intron variant Mapped gene(s): CEP120 Associations 1 Studies 1 |
V rs890928 | |||
Location: 5:123360673 Cytogenetic region:5q23.2 Most severe consequence: Intron variant Mapped gene(s): CEP120 Associations 1 Studies 1 |
V rs13156123 | |||
Location: 5:123396356 Cytogenetic region:5q23.2 Most severe consequence: Intron variant Mapped gene(s): CEP120 Associations 1 Studies 1 |
V rs147987632 | |||
Location: 5:123414694 Cytogenetic region:5q23.2 Most severe consequence: Intron variant Mapped gene(s): CEP120 Associations 1 Studies 1 |
V rs4267865 | |||
Location: 5:123368648 Cytogenetic region:5q23.2 Most severe consequence: Intron variant Mapped gene(s): CEP120 Associations 2 Studies 2 |
V rs7706501 | |||
Location: 5:123419782 Cytogenetic region:5q23.2 Most severe consequence: Intron variant Mapped gene(s): CEP120 Associations 1 Studies 1 |
V rs4836533 | |||
Location: 5:123348870 Cytogenetic region:5q23.2 Most severe consequence: Intron variant Mapped gene(s): CEP120 Associations 1 Studies 1 |
V rs7713551 | |||
Location: 5:123385559 Cytogenetic region:5q23.2 Most severe consequence: Intron variant Mapped gene(s): CEP120 Associations 1 Studies 1 |
V rs17150407 | |||
Location: 5:123388973 Cytogenetic region:5q23.2 Most severe consequence: Intron variant Mapped gene(s): CEP120 Associations 1 Studies 1 |
V rs6884993 | |||
Location: 5:123410834 Cytogenetic region:5q23.2 Most severe consequence: Intron variant Mapped gene(s): CEP120 Associations 1 Studies 1 |
V rs10478580 | |||
Location: 5:123375474 Cytogenetic region:5q23.2 Most severe consequence: Intron variant Mapped gene(s): CEP120 Associations 1 Studies 1 |
V rs1428387 | |||
Location: 5:123369550 Cytogenetic region:5q23.2 Most severe consequence: Intron variant Mapped gene(s): CEP120 Associations 1 Studies 1 |
V rs11953651 | |||
Location: 5:123422024 Cytogenetic region:5q23.2 Most severe consequence: Intron variant Mapped gene(s): CEP120 Associations 2 Studies 2 |
V rs2303719 | |||
Location: 5:123346460 Cytogenetic region:5q23.2 Most severe consequence: 3 prime utr variant Mapped gene(s): CEP120 Associations 1 Studies 1 |
V rs7711753 | |||
Location: 5:123397623 Cytogenetic region:5q23.2 Most severe consequence: Intron variant Mapped gene(s): CEP120 Associations 2 Studies 2 |
V rs566909063 | |||
Location: 5:123419554 Cytogenetic region:5q23.2 Most severe consequence: Intron variant Mapped gene(s): CEP120 Associations 1 Studies 1 |
V rs62377764 | |||
Location: 5:123418732 Cytogenetic region:5q23.2 Most severe consequence: Intron variant Mapped gene(s): CEP120 Associations 1 Studies 1 |
V rs1428381 | |||
Location: 5:123358207 Cytogenetic region:5q23.2 Most severe consequence: Intron variant Mapped gene(s): CEP120 Associations 1 Studies 1 |
V rs1047440 | |||
Location: 5:123346140 Cytogenetic region:5q23.2 Most severe consequence: 3 prime utr variant Mapped gene(s): CEP120 Associations 5 Studies 5 |
V rs34984032 | |||
Location: 5:123356960 Cytogenetic region:5q23.2 Most severe consequence: Intron variant Mapped gene(s): CEP120 Associations 2 Studies 2 |
V rs13154356 | |||
Location: 5:123408484 Cytogenetic region:5q23.2 Most severe consequence: Intron variant Mapped gene(s): CEP120 Associations 1 Studies 1 |
V rs4836008 | |||
Location: 5:123409597 Cytogenetic region:5q23.2 Most severe consequence: Intron variant Mapped gene(s): CEP120 Associations 1 Studies 1 |
V rs2162826 | |||
Location: 5:123378783 Cytogenetic region:5q23.2 Most severe consequence: Intron variant Mapped gene(s): CEP120 Associations 1 Studies 1 |
V rs12520233 | |||
Location: 5:123345585 Cytogenetic region:5q23.2 Most severe consequence: 3 prime utr variant Mapped gene(s): CEP120 Associations 2 Studies 2 |
V rs13159477 | |||
Location: 5:123385229 Cytogenetic region:5q23.2 Most severe consequence: Intron variant Mapped gene(s): CEP120 Associations 1 Studies 1 |
V rs6860168 | |||
Location: 5:123395874 Cytogenetic region:5q23.2 Most severe consequence: Intron variant Mapped gene(s): CEP120 Associations 1 Studies 1 |
V rs2115173 | |||
Location: 5:123349654 Cytogenetic region:5q23.2 Most severe consequence: Intron variant Mapped gene(s): CEP120 Associations 1 Studies 1 |
V rs12655753 | |||
Location: 5:123347118 Cytogenetic region:5q23.2 Most severe consequence: Intron variant Mapped gene(s): CEP120 Associations 4 Studies 4 |
V rs17470137 | |||
Location: 5:123195653 Cytogenetic region:5q23.2 Most severe consequence: Intergenic variant Mapped gene(s): CEP120,PRDM6 Associations 6 Studies 6 |
V rs7705033 | |||
Location: 5:123439091 Cytogenetic region:5q23.2 Most severe consequence: Regulatory region variant Mapped gene(s): HMGB3P17,CEP120 Associations 1 Studies 1 |
V rs6881280 | |||
Location: 5:123279830 Cytogenetic region:5q23.2 Most severe consequence: Intergenic variant Mapped gene(s): CEP120,PRDM6 Associations 1 Studies 1 |
V rs1582931 | |||
Location: 5:123321505 Cytogenetic region:5q23.2 Most severe consequence: Intergenic variant Mapped gene(s): CEP120,PRDM6 Associations 13 Studies 13 |
V rs7708474 | |||
Location: 5:123340831 Cytogenetic region:5q23.2 Most severe consequence: Intergenic variant Mapped gene(s): CEP120,PRDM6 Associations 1 Studies 1 |
V rs11241696 | |||
Location: 5:123424168 Cytogenetic region:5q23.2 Most severe consequence: Intergenic variant Mapped gene(s): HMGB3P17,CEP120 Associations 1 Studies 1 |
V rs75887402 | |||
Location: 5:123338869 Cytogenetic region:5q23.2 Most severe consequence: Intergenic variant Mapped gene(s): CEP120,PRDM6 Associations 3 Studies 3 |
V rs2081914 | |||
Location: 5:123337928 Cytogenetic region:5q23.2 Most severe consequence: Intergenic variant Mapped gene(s): CEP120,PRDM6 Associations 1 Studies 1 |
V rs337100 | |||
Location: 5:123210816 Cytogenetic region:5q23.2 Most severe consequence: Intergenic variant Mapped gene(s): CEP120,PRDM6 Associations 2 Studies 1 |
V rs4308481 | |||
Location: 5:123316412 Cytogenetic region:5q23.2 Most severe consequence: Intergenic variant Mapped gene(s): CEP120,PRDM6 Associations 13 Studies 13 |
V rs62377770 | |||
Location: 5:123453558 Cytogenetic region:5q23.2 Most severe consequence: Intergenic variant Mapped gene(s): HMGB3P17,CEP120 Associations 1 Studies 1 |
V rs112446794 | |||
Location: 5:123329771 Cytogenetic region:5q23.2 Most severe consequence: Intergenic variant Mapped gene(s): CEP120,PRDM6 Associations 1 Studies 1 |
V rs9784689 | |||
Location: 5:123324302 Cytogenetic region:5q23.2 Most severe consequence: Intergenic variant Mapped gene(s): CEP120,PRDM6 Associations 1 Studies 1 |
V rs11241697 | |||
Location: 5:123427510 Cytogenetic region:5q23.2 Most severe consequence: Intergenic variant Mapped gene(s): HMGB3P17,CEP120 Associations 1 Studies 1 |
V rs144052331 | |||
Location: 5:123315191 Cytogenetic region:5q23.2 Most severe consequence: Intergenic variant Mapped gene(s): CEP120,PRDM6 Associations 1 Studies 1 |
V rs200525873 | |||
Location: 5:123317220 Cytogenetic region:5q23.2 Most severe consequence: Intergenic variant Mapped gene(s): CEP120,PRDM6 Associations 1 Studies 1 |
V rs13165542 | |||
Location: 5:123433602 Cytogenetic region:5q23.2 Most severe consequence: Intergenic variant Mapped gene(s): HMGB3P17,CEP120 Associations 2 Studies 2 |
V rs71574104 | |||
Location: 5:123401746 Cytogenetic region:5q23.2 Most severe consequence: Intron variant Mapped gene(s): CEP120,KRT8P33 Associations 1 Studies 1 |
V rs11437038 | |||
Location: 5:123314356 Cytogenetic region:5q23.2 Most severe consequence: Intergenic variant Mapped gene(s): CEP120,PRDM6 Associations 1 Studies 1 |
V rs34824900 | |||
Location: 5:123341914 Cytogenetic region:5q23.2 Most severe consequence: Intergenic variant Mapped gene(s): CEP120,PRDM6 Associations 1 Studies 1 |
V rs77097530 | |||
Location: 5:123274159 Cytogenetic region:5q23.2 Most severe consequence: Intergenic variant Mapped gene(s): CEP120,PRDM6 Associations 3 Studies 3 |
V rs74790763 | |||
Location: 5:123339520 Cytogenetic region:5q23.2 Most severe consequence: Intergenic variant Mapped gene(s): CEP120,PRDM6 Associations 2 Studies 2 |
V rs337086 | |||
Location: 5:123219807 Cytogenetic region:5q23.2 Most severe consequence: Intergenic variant Mapped gene(s): CEP120,PRDM6 Associations 1 Studies 1 |
V rs7705127 | |||
Location: 5:123305008 Cytogenetic region:5q23.2 Most severe consequence: Intergenic variant Mapped gene(s): CEP120,PRDM6 Associations 1 Studies 1 |
V rs1962848 | |||
Location: 5:123335966 Cytogenetic region:5q23.2 Most severe consequence: Intergenic variant Mapped gene(s): CEP120,PRDM6 Associations 2 Studies 2 |
V rs571326882 | |||
Location: 5:123278148 Cytogenetic region:5q23.2 Most severe consequence: Intergenic variant Mapped gene(s): CEP120,PRDM6 Associations 1 Studies 1 |
V rs337101 | |||
Location: 5:123214952 Cytogenetic region:5q23.2 Most severe consequence: Intergenic variant Mapped gene(s): CEP120,PRDM6 Associations 4 Studies 4 |
V rs7702622 | |||
Location: 5:123213027 Cytogenetic region:5q23.2 Most severe consequence: Intergenic variant Mapped gene(s): CEP120,PRDM6 Associations 2 Studies 2 |
V rs34909326 | |||
Location: 5:123295991 Cytogenetic region:5q23.2 Most severe consequence: Intergenic variant Mapped gene(s): CEP120,PRDM6 Associations 2 Studies 2 |
V rs139034638 | |||
Location: 5:123242333 Cytogenetic region:5q23.2 Most severe consequence: Regulatory region variant Mapped gene(s): CEP120,PRDM6 Associations 1 Studies 1 |
V rs13156484 | |||
Location: 5:123317705 Cytogenetic region:5q23.2 Most severe consequence: Intergenic variant Mapped gene(s): CEP120,PRDM6 Associations 3 Studies 3 |
V rs919305 | |||
Location: 5:123291687 Cytogenetic region:5q23.2 Most severe consequence: Intergenic variant Mapped gene(s): CEP120,PRDM6 Associations 1 Studies 1 |
V rs1835009 | |||
Location: 5:123325523 Cytogenetic region:5q23.2 Most severe consequence: Intergenic variant Mapped gene(s): CEP120,PRDM6 Associations 1 Studies 1 |
V rs13170405 | |||
Location: 5:123443425 Cytogenetic region:5q23.2 Most severe consequence: Intergenic variant Mapped gene(s): HMGB3P17,CEP120 Associations 1 Studies 1 |
V rs79274348 | |||
Location: 5:123435918 Cytogenetic region:5q23.2 Most severe consequence: Intergenic variant Mapped gene(s): HMGB3P17,CEP120 Associations 1 Studies 1 |
V rs13162125 | |||
Location: 5:123429803 Cytogenetic region:5q23.2 Most severe consequence: Intergenic variant Mapped gene(s): HMGB3P17,CEP120 Associations 1 Studies 1 |
V rs534050929 | |||
Location: 5:123331342 Cytogenetic region:5q23.2 Most severe consequence: Intergenic variant Mapped gene(s): CEP120,PRDM6 Associations 1 Studies 1 |
V rs6891483 | |||
Location: 5:123324270 Cytogenetic region:5q23.2 Most severe consequence: Intergenic variant Mapped gene(s): CEP120,PRDM6 Associations 1 Studies 1 |
V rs34074238 (rs558113277) | |||
Location: 5:123407106 Cytogenetic region:5q23.2 Most severe consequence: Intron variant Mapped gene(s): CEP120 Associations 1 Studies 1 |
V rs6894334 | |||
Location: 5:123299671 Cytogenetic region:5q23.2 Most severe consequence: Intergenic variant Mapped gene(s): CEP120,PRDM6 Associations 2 Studies 2 |
V rs62377767 | |||
Location: 5:123425370 Cytogenetic region:5q23.2 Most severe consequence: Intergenic variant Mapped gene(s): HMGB3P17,CEP120 Associations 4 Studies 4 |
V rs62378779 | |||
Location: 5:123313596 Cytogenetic region:5q23.2 Most severe consequence: Intergenic variant Mapped gene(s): CEP120,PRDM6 Associations 2 Studies 2 |
V rs11955337 | |||
Location: 5:123458438 Cytogenetic region:5q23.2 Most severe consequence: Intergenic variant Mapped gene(s): HMGB3P17,CEP120 Associations 3 Studies 3 |
V rs6875307 | |||
Location: 5:123461540 Cytogenetic region:5q23.2 Most severe consequence: Intergenic variant Mapped gene(s): HMGB3P17,CEP120 Associations 1 Studies 1 |
V rs338796 | |||
Location: 5:123227106 Cytogenetic region:5q23.2 Most severe consequence: Intergenic variant Mapped gene(s): CEP120,PRDM6 Associations 1 Studies 1 |
V rs70988580 (rs756395458) | |||
Location: 5:123440363 Cytogenetic region:5q23.2 Most severe consequence: Intergenic variant Mapped gene(s): HMGB3P17,CEP120 Associations 1 Studies 1 |