Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs35443 12 115115073 intergenic variant G/C snv 0.40 5
rs509728 11 116662450 downstream gene variant G/C snv 2.7E-02 5
rs6108787 20 10986566 intron variant T/G snv 0.46 5
rs10750766 11 65706327 regulatory region variant C/A snv 0.60 4
rs11967262 6 43792590 intergenic variant C/G snv 0.41 4
rs1275984 2 26688641 upstream gene variant A/C;G snv 4
rs1689040 12 89584456 intron variant C/G;T snv 4
rs2392929 7 106773623 upstream gene variant T/A;C;G snv 4
rs2484294 10 114032303 intergenic variant G/A snv 0.70 4
rs2972143 1.000 0.080 2 226251649 intergenic variant A/G snv 0.67 4
rs4277405 17 63471557 upstream gene variant C/T snv 0.63 4
rs5014650 6 160678471 upstream gene variant G/A snv 0.16 4
rs6073958 20 45923216 downstream gene variant T/C snv 0.22 4
rs72640287 1 11905735 upstream gene variant C/T snv 2.6E-02 4
rs10713774 4 26048829 intergenic variant C/- del 0.18 3
rs10734252 1.000 0.080 11 17383292 non coding transcript exon variant G/A snv 0.71 3
rs10761716 10 63122540 downstream gene variant C/G snv 0.40 3
rs10826334 10 59620724 intron variant C/A;G snv 3
rs11072518 15 74942269 upstream gene variant T/A;C snv 3
rs1275985 2 26688877 upstream gene variant C/T snv 0.50 3
rs13280442 8 11610048 intergenic variant C/A;G snv 3
rs1848797 10 62793174 intron variant A/G snv 0.27 3
rs1943940 18 74037957 upstream gene variant T/C snv 0.42 3
rs2328223 20 17865277 intergenic variant A/C;G;T snv 3
rs2908522 6 139514262 intron variant C/G snv 0.52 3