Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1033198 11 1325572 intergenic variant T/A;C;G snv 1
rs10751635 11 1062990 intergenic variant A/G snv 0.41 1
rs10794278 11 1061718 intergenic variant G/T snv 0.32 1
rs10794279 11 1061781 intergenic variant C/T snv 0.32 1
rs10794280 11 1062867 intergenic variant C/T snv 0.30 1
rs10794284 11 1067011 intergenic variant G/A snv 0.34 1
rs10902073 11 1060934 TF binding site variant C/A snv 0.31 1
rs11858744 15 85339833 regulatory region variant C/T snv 0.40 1
rs12417955 11 1262997 downstream gene variant A/G snv 0.55 0.54 1
rs1453184 15 40437201 upstream gene variant A/G snv 0.59 1
rs1997392 3 169791864 upstream gene variant C/T snv 0.33 1
rs2301160 11 1063767 intergenic variant T/C snv 0.41 1
rs2334659 11 1335833 non coding transcript exon variant G/A snv 0.11 1
rs3129868 6 32436600 upstream gene variant A/C snv 0.89 1
rs4077759 11 1112068 downstream gene variant C/T snv 0.53 1
rs6974373 7 99993270 upstream gene variant C/A;G snv 1
rs7118481 11 1327108 regulatory region variant G/A;C;T snv 1
rs7625734 3 169791127 upstream gene variant T/A;C;G snv 1
rs549977217
ABCA3
16 2284869 missense variant C/T snv 4.6E-04 1.0E-04 1
rs768483175
ABCA3
16 2319832 missense variant G/A snv 2.4E-05 7.0E-06 1
rs879159551
ABCA3
16 2319811 missense variant G/T snv 1
rs9860874
ACTRT3
3 169768483 intron variant C/A snv 0.33 1
rs12438724
ADAMTS7P4
15 85282062 intron variant C/T snv 0.41 1
rs16941432
AKAP13
15 85559945 intron variant A/G snv 0.37 1
rs2169877
AKAP13
15 85542571 intron variant G/A snv 0.70 1