G AP3D1 | |||
Description: adaptor related protein complex 3 subunit delta 1 Associations 96 Studies 86 |
P A genome-wide association study identifies PLCL2 and AP3D1-DOT1L-SF3A2 as new susceptibility loci for myocardial infarction in Japanese. | |||
Hirokawa M et al. 2014 Eur J Hum Genet PMID:24916648 Associations 4 Studies 1 |
V rs3803915 | |||
Location: 19:2160530 Cytogenetic region:19p13.3 Most severe consequence: Intergenic variant Mapped gene(s): AP3D1 Associations 3 Studies 3 |
V rs57908212 | |||
Location: 19:2161322 Cytogenetic region:19p13.3 Most severe consequence: Intergenic variant Mapped gene(s): AP3D1 Associations 7 Studies 7 |
V rs62128375 | |||
Location: 19:2119319 Cytogenetic region:19p13.3 Most severe consequence: Intron variant Mapped gene(s): AP3D1 Associations 1 Studies 1 |
V rs25673 | |||
Location: 19:2109158 Cytogenetic region:19p13.3 Most severe consequence: Missense variant Mapped gene(s): AP3D1 Associations 1 Studies 1 |
V rs75483641 | |||
Location: 19:2123929 Cytogenetic region:19p13.3 Most severe consequence: Intron variant Mapped gene(s): AP3D1 Associations 2 Studies 2 |
V rs4807203 | |||
Location: 19:2127273 Cytogenetic region:19p13.3 Most severe consequence: Intron variant Mapped gene(s): AP3D1 Associations 2 Studies 2 |
V rs183203602 | |||
Location: 19:2154724 Cytogenetic region:19p13.3 Most severe consequence: Regulatory region variant Mapped gene(s): AP3D1 Associations 2 Studies 2 |
V rs188076989 | |||
Location: 19:2120460 Cytogenetic region:19p13.3 Most severe consequence: Intron variant Mapped gene(s): AP3D1 Associations 2 Studies 2 |
V rs7249081 | |||
Location: 19:2157168 Cytogenetic region:19p13.3 Most severe consequence: Intergenic variant Mapped gene(s): AP3D1 Associations 12 Studies 11 |
V rs12985850 | |||
Location: 19:2155043 Cytogenetic region:19p13.3 Most severe consequence: Regulatory region variant Mapped gene(s): AP3D1 Associations 4 Studies 4 |
V rs8102624 | |||
Location: 19:2161444 Cytogenetic region:19p13.3 Most severe consequence: Regulatory region variant Mapped gene(s): AP3D1 Associations 17 Studies 17 |
V rs35917214 | |||
Location: 19:2135715 Cytogenetic region:19p13.3 Most severe consequence: Intron variant Mapped gene(s): AP3D1 Associations 2 Studies 2 |
V rs8106338 | |||
Location: 19:2103187 Cytogenetic region:19p13.3 Most severe consequence: Intron variant Mapped gene(s): AP3D1 Associations 1 Studies 1 |
V rs36065733 | |||
Location: 19:2163772 Cytogenetic region:19p13.3 Most severe consequence: Regulatory region variant Mapped gene(s): AP3D1 Associations 7 Studies 7 |
V rs146657690 | |||
Location: 19:2153901 Cytogenetic region:19p13.3 Most severe consequence: Intergenic variant Mapped gene(s): AP3D1 Associations 1 Studies 1 |
V rs34656141 | |||
Location: 19:2158229 Cytogenetic region:19p13.3 Most severe consequence: Intergenic variant Mapped gene(s): AP3D1 Associations 2 Studies 2 |
V rs147018632 | |||
Location: 19:2151516 Cytogenetic region:19p13.3 Most severe consequence: 5 prime utr variant Mapped gene(s): AP3D1 Associations 1 Studies 1 |
V rs4806831 | |||
Location: 19:2136704 Cytogenetic region:19p13.3 Most severe consequence: Intron variant Mapped gene(s): AP3D1 Associations 1 Studies 1 |
V rs72983502 | |||
Location: 19:2156955 Cytogenetic region:19p13.3 Most severe consequence: Intergenic variant Mapped gene(s): AP3D1 Associations 1 Studies 1 |
V rs6510645 | |||
Location: 19:2158399 Cytogenetic region:19p13.3 Most severe consequence: Intergenic variant Mapped gene(s): AP3D1 Associations 1 Studies 1 |
V rs35976665 | |||
Location: 19:2131676 Cytogenetic region:19p13.3 Most severe consequence: Intron variant Mapped gene(s): AP3D1 Associations 3 Studies 3 |
V rs12973528 | |||
Location: 19:2155498 Cytogenetic region:19p13.3 Most severe consequence: Intergenic variant Mapped gene(s): AP3D1 Associations 3 Studies 3 |
V rs12985258 | |||
Location: 19:2159572 Cytogenetic region:19p13.3 Most severe consequence: Intergenic variant Mapped gene(s): AP3D1 Associations 1 Studies 1 |
V rs144821294 | |||
Location: 19:2155137 Cytogenetic region:19p13.3 Most severe consequence: Intergenic variant Mapped gene(s): AP3D1 Associations 2 Studies 2 |
V rs1074047 | |||
Location: 19:2158749 Cytogenetic region:19p13.3 Most severe consequence: Intergenic variant Mapped gene(s): AP3D1 Associations 5 Studies 5 |
V rs1017084 | |||
Location: 19:2128055 Cytogenetic region:19p13.3 Most severe consequence: Intron variant Mapped gene(s): AP3D1 Associations 1 Studies 1 |
V rs2240655 | |||
Location: 19:2115791 Cytogenetic region:19p13.3 Most severe consequence: Intron variant Mapped gene(s): AP3D1 Associations 1 Studies 1 |
V rs2240653 | |||
Location: 19:2115037 Cytogenetic region:19p13.3 Most severe consequence: Intron variant Mapped gene(s): AP3D1 Associations 1 Studies 1 |
V rs4807201 | |||
Location: 19:2120315 Cytogenetic region:19p13.3 Most severe consequence: Intron variant Mapped gene(s): AP3D1 Associations 1 Studies 1 |
V rs112663739 | |||
Location: 19:2157238 Cytogenetic region:19p13.3 Most severe consequence: Intergenic variant Mapped gene(s): AP3D1 Associations 1 Studies 1 |
V rs145968810 | |||
Location: 19:2156643 Cytogenetic region:19p13.3 Most severe consequence: Intergenic variant Mapped gene(s): AP3D1 Associations 1 Studies 1 |
V rs12971884 | |||
Location: 19:2160260 Cytogenetic region:19p13.3 Most severe consequence: Intergenic variant Mapped gene(s): AP3D1 Associations 2 Studies 2 |
V rs2385543 | |||
Location: 19:2162640 Cytogenetic region:19p13.3 Most severe consequence: Intergenic variant Mapped gene(s): AP3D1 Associations 2 Studies 2 |
V rs35751290 | |||
Location: 19:2139358 Cytogenetic region:19p13.3 Most severe consequence: Intron variant Mapped gene(s): AP3D1 Associations 1 Studies 1 |
V rs12985346 | |||
Location: 19:2164352 Cytogenetic region:19p13.3 Most severe consequence: Intron variant Mapped gene(s): DOT1L,AP3D1 Associations 1 Studies 1 |