G ELP1 | |||
Description: elongator acetyltransferase complex subunit 1 Associations 29 Studies 28 |
V rs12353209 | |||
Location: 9:108890800 Cytogenetic region:9q31.3 Most severe consequence: Intron variant Mapped gene(s): ELP1 Associations 1 Studies 1 |
V rs16913693 | |||
Location: 9:108918079 Cytogenetic region:9q31.3 Most severe consequence: Intron variant Mapped gene(s): ELP1 Associations 5 Studies 5 |
V rs2275641 | |||
Location: 9:108934109 Cytogenetic region:9q31.3 Most severe consequence: 5 prime utr variant Mapped gene(s): ELP1 Associations 3 Studies 3 |
V rs10979613 | |||
Location: 9:108925304 Cytogenetic region:9q31.3 Most severe consequence: Intron variant Mapped gene(s): ELP1 Associations 1 Studies 1 |
V rs1341215 | |||
Location: 9:108900070 Cytogenetic region:9q31.3 Most severe consequence: Intron variant Mapped gene(s): ELP1 Associations 3 Studies 3 |
V rs3818932 | |||
Location: 9:108901898 Cytogenetic region:9q31.3 Most severe consequence: Intron variant Mapped gene(s): ELP1 Associations 1 Studies 1 |
V rs11788336 | |||
Location: 9:108926107 Cytogenetic region:9q31.3 Most severe consequence: Intron variant Mapped gene(s): ELP1 Associations 1 Studies 1 |
V rs1981267 | |||
Location: 9:108875052 Cytogenetic region:9q31.3 Most severe consequence: Intron variant Mapped gene(s): ELP1 Associations 1 Studies 1 |
V rs17853166 | |||
Location: 9:108917660 Cytogenetic region:9q31.3 Most severe consequence: Missense variant Mapped gene(s): ELP1 Associations 2 Studies 2 |
V rs838827 | |||
Location: 9:108906372 Cytogenetic region:9q31.3 Most severe consequence: Missense variant Mapped gene(s): ELP1 Associations 1 Studies 1 |
V rs4978760 | |||
Location: 9:108898870 Cytogenetic region:9q31.3 Most severe consequence: Intron variant Mapped gene(s): ELP1 Associations 4 Studies 4 |
V rs10979605 | |||
Location: 9:108901513 Cytogenetic region:9q31.3 Most severe consequence: Synonymous variant Mapped gene(s): ELP1 Associations 1 Studies 1 |
V rs3763643 | |||
Location: 9:108933327 Cytogenetic region:9q31.3 Most severe consequence: Intron variant Mapped gene(s): ELP1 Associations 1 Studies 1 |
V rs78490371 | |||
Location: 9:108907695 Cytogenetic region:9q31.3 Most severe consequence: Intron variant Mapped gene(s): ELP1 Associations 1 Studies 1 |
V rs3750457 | |||
Location: 9:108922709 Cytogenetic region:9q31.3 Most severe consequence: Intron variant Mapped gene(s): ELP1 Associations 1 Studies 1 |
V rs3780510 | |||
Location: 9:108891888 Cytogenetic region:9q31.3 Most severe consequence: Intron variant Mapped gene(s): ELP1 Associations 1 Studies 1 |
V rs117634551 | |||
Location: 9:108934366 Cytogenetic region:9q31.3 Most severe consequence: Regulatory region variant Mapped gene(s): ELP1,ABITRAM Associations 1 Studies 1 |