G RFT1 | |||
Description: RFT1 homolog Associations 67 Studies 56 |
V rs2336725 | |||
Location: 3:53084723 Cytogenetic region:3p21.1 Most severe consequence: Intron variant Mapped gene(s): RFT1 Associations 1 Studies 1 |
V rs2564921 | |||
Location: 3:53091569 Cytogenetic region:3p21.1 Most severe consequence: 3 prime utr variant Mapped gene(s): RFT1 Associations 2 Studies 2 |
V rs13088281 | |||
Location: 3:53113560 Cytogenetic region:3p21.1 Most severe consequence: Intron variant Mapped gene(s): RFT1 Associations 1 Studies 1 |
V rs11242 | |||
Location: 3:53091906 Cytogenetic region:3p21.1 Most severe consequence: Synonymous variant Mapped gene(s): RFT1 Associations 5 Studies 3 |
V rs2115780 | |||
Location: 3:53108964 Cytogenetic region:3p21.1 Most severe consequence: Intron variant Mapped gene(s): RFT1 Associations 1 Studies 1 |
V rs2581828 | |||
Location: 3:53099133 Cytogenetic region:3p21.1 Most severe consequence: Intron variant Mapped gene(s): RFT1 Associations 5 Studies 4 |
V rs62255930 | |||
Location: 3:53097261 Cytogenetic region:3p21.1 Most severe consequence: Intron variant Mapped gene(s): RFT1 Associations 1 Studies 1 |
V rs2163167 | |||
Location: 3:53097756 Cytogenetic region:3p21.1 Most severe consequence: Intron variant Mapped gene(s): RFT1 Associations 1 Studies 1 |
V rs2564923 | |||
Location: 3:53069246 Cytogenetic region:3p21.1 Most severe consequence: Intron variant Mapped gene(s): RFT1 Associations 5 Studies 5 |
V rs2581787 | |||
Location: 3:53093661 Cytogenetic region:3p21.1 Most severe consequence: Intron variant Mapped gene(s): RFT1 Associations 3 Studies 3 |
V rs2253675 | |||
Location: 3:53085518 Cytogenetic region:3p21.1 Most severe consequence: Intron variant Mapped gene(s): RFT1 Associations 1 Studies 1 |
V rs9838517 | |||
Location: 3:53110347 Cytogenetic region:3p21.1 Most severe consequence: Intron variant Mapped gene(s): RFT1 Associations 2 Studies 2 |
V rs1004807 | |||
Location: 3:53106587 Cytogenetic region:3p21.1 Most severe consequence: Intron variant Mapped gene(s): RFT1 Associations 3 Studies 3 |
V rs62255926 | |||
Location: 3:53091413 Cytogenetic region:3p21.1 Most severe consequence: 3 prime utr variant Mapped gene(s): RFT1 Associations 1 Studies 1 |
V rs2564942 | |||
Location: 3:53105490 Cytogenetic region:3p21.1 Most severe consequence: Intron variant Mapped gene(s): RFT1 Associations 1 Studies 1 |
V rs2564922 | |||
Location: 3:53091453 Cytogenetic region:3p21.1 Most severe consequence: 3 prime utr variant Mapped gene(s): RFT1 Associations 1 Studies 1 |
V rs6769944 | |||
Location: 3:53126227 Cytogenetic region:3p21.1 Most severe consequence: Intron variant Mapped gene(s): RFT1 Associations 1 Studies 1 |
V rs11713763 | |||
Location: 3:53126344 Cytogenetic region:3p21.1 Most severe consequence: Intron variant Mapped gene(s): RFT1 Associations 4 Studies 4 |
V rs1560333 | |||
Location: 3:53104238 Cytogenetic region:3p21.1 Most severe consequence: Intron variant Mapped gene(s): RFT1 Associations 1 Studies 1 |
V rs13084937 | |||
Location: 3:53070623 Cytogenetic region:3p21.1 Most severe consequence: Intron variant Mapped gene(s): RFT1 Associations 1 Studies 1 |
V rs2581774 | |||
Location: 3:53105491 Cytogenetic region:3p21.1 Most severe consequence: Intron variant Mapped gene(s): RFT1 Associations 1 Studies 1 |
V rs2336723 | |||
Location: 3:53072031 Cytogenetic region:3p21.1 Most severe consequence: Intron variant Mapped gene(s): RFT1 Associations 1 Studies 1 |
V rs148752275 | |||
Location: 3:53113435 Cytogenetic region:3p21.1 Most severe consequence: Intron variant Mapped gene(s): RFT1 Associations 1 Studies 1 |
V rs2581782 | |||
Location: 3:53088241 Cytogenetic region:3p21.1 Most severe consequence: Intron variant Mapped gene(s): RFT1 Associations 1 Studies 1 |
V rs2581799 | |||
Location: 3:53074760 Cytogenetic region:3p21.1 Most severe consequence: Intron variant Mapped gene(s): RFT1 Associations 2 Studies 2 |
V rs11713926 | |||
Location: 3:53121056 Cytogenetic region:3p21.1 Most severe consequence: Intron variant Mapped gene(s): RFT1 Associations 1 Studies 1 |
V rs6786405 | |||
Location: 3:53076196 Cytogenetic region:3p21.1 Most severe consequence: Intron variant Mapped gene(s): RFT1 Associations 1 Studies 1 |
V rs7615099 | |||
Location: 3:53109885 Cytogenetic region:3p21.1 Most severe consequence: Intron variant Mapped gene(s): RFT1 Associations 2 Studies 2 |
V rs2564940 | |||
Location: 3:53073553 Cytogenetic region:3p21.1 Most severe consequence: Intron variant Mapped gene(s): RFT1 Associations 2 Studies 2 |
V rs4687701 | |||
Location: 3:53087260 Cytogenetic region:3p21.1 Most severe consequence: Intron variant Mapped gene(s): RFT1 Associations 2 Studies 2 |
V rs9874517 | |||
Location: 3:53094355 Cytogenetic region:3p21.1 Most severe consequence: Intron variant Mapped gene(s): RFT1 Associations 1 Studies 1 |
V rs35783750 | |||
Location: 3:53100847 Cytogenetic region:3p21.1 Most severe consequence: Intron variant Mapped gene(s): RFT1 Associations 1 Studies 1 |
V rs6770152 | |||
Location: 3:53066198 Cytogenetic region:3p21.1 Most severe consequence: Intron variant Mapped gene(s): RFT1,SERBP1P3 Associations 4 Studies 3 |
V rs1080500 | |||
Location: 3:53141001 Cytogenetic region:3p21.1 Most severe consequence: Regulatory region variant Mapped gene(s): RFT1,PRKCD Associations 2 Studies 2 |
V rs6445559 | |||
Location: 3:53065450 Cytogenetic region:3p21.1 Most severe consequence: Intron variant Mapped gene(s): RFT1,SERBP1P3 Associations 3 Studies 3 |
V rs7637082 | |||
Location: 3:53065645 Cytogenetic region:3p21.1 Most severe consequence: Intron variant Mapped gene(s): RFT1,SERBP1P3 Associations 1 Studies 1 |