Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7424771
RBMS1
2 160419867 intron variant G/A snv 0.44 4
rs117068593
RIN3
14 92651884 missense variant C/T snv 0.13 0.11 4
rs7752448
ZSCAN31
6 28333322 intron variant A/G snv 0.15 4
rs1102077 6 139950220 intron variant A/C snv 0.21 3
rs11176001 12 66015587 regulatory region variant C/A snv 9.6E-02 3
rs117642368 17 45321692 upstream gene variant G/C snv 6.9E-02 3
rs1192415 0.925 0.040 1 91611540 TF binding site variant G/A snv 0.81 3
rs12198986 6 7719826 regulatory region variant G/A snv 0.37 3
rs12331869 4 55145982 intergenic variant A/G snv 0.76 3
rs12481092 20 46858178 upstream gene variant C/T snv 0.21 3
rs12698403 7 156334552 intergenic variant G/A snv 0.40 3
rs12707691 7 84940194 non coding transcript exon variant C/G snv 0.24 3
rs12811814 12 4134583 intergenic variant T/C snv 0.45 3
rs12945803 17 48474867 upstream gene variant T/C snv 0.19 3
rs2353940 4 144819746 intron variant T/C snv 0.16 3
rs2555019 1.000 0.040 12 114230813 intergenic variant T/C;G snv 3
rs2701110 12 114232065 intergenic variant C/A snv 0.14 3
rs35043843 1 118368672 intergenic variant T/G snv 0.21 3
rs41310284 10 100687890 intergenic variant C/A;T snv 3
rs4866846 5 43976060 intergenic variant A/G snv 0.76 3
rs6501455 17 71205670 upstream gene variant A/G snv 0.40 3
rs7465401 8 69455013 intergenic variant T/C snv 0.29 3
rs879394 3 168992055 regulatory region variant G/T snv 0.24 3
rs9385988 6 142239820 intergenic variant A/G snv 0.27 3
rs12513481
AP3B1
5 78155004 intron variant G/C snv 0.19 3