Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs117078022 8 46517978 intergenic variant T/C snv 1.7E-02 1
rs117407105 2 136168220 regulatory region variant A/C;G snv 1
rs11747786 5 72808588 intron variant G/A snv 0.47 1
rs11758031 6 33716581 upstream gene variant G/A snv 0.15 1
rs117977586 7 92952842 intergenic variant A/G snv 1.7E-02 1
rs11895277 2 71850830 intergenic variant C/T snv 0.80 1
rs11901428 2 30215974 intergenic variant G/A snv 0.32 1
rs12113288 7 76291498 downstream gene variant G/A snv 0.35 1
rs12362717 11 55093446 intergenic variant C/A;G;T snv 1
rs12403425 1 197845693 intergenic variant C/A snv 0.17 1
rs12432697 14 37584129 intergenic variant G/T snv 0.18 1
rs12581511 12 46180005 downstream gene variant C/G snv 0.14 1
rs12613485 2 101538302 intron variant G/A snv 8.9E-02 1
rs1263602 2 207063398 intergenic variant T/A;G snv 1
rs12724990 1 100671474 intergenic variant G/A;C snv 1
rs12759042 1 12045275 intergenic variant T/G snv 0.22 1
rs12897672 14 20963254 upstream gene variant C/T snv 0.22 1
rs12925999 16 51203865 intron variant T/A;G snv 1
rs1297597 12 113012395 intron variant A/G snv 0.77 1
rs13032656 2 212823634 intron variant A/G snv 0.53 1
rs13089722 3 128587914 regulatory region variant G/A snv 0.11 1
rs13138280 4 89125697 intergenic variant G/A;C snv 1
rs13274067 8 80355001 intron variant G/A;C;T snv 1
rs13295248 9 136492188 downstream gene variant T/C snv 0.21 1
rs1353286 3 27730523 intergenic variant T/G snv 0.60 1