Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10118552 9 90004338 intron variant A/G snv 0.59 1
rs1013910 1 116868761 intergenic variant G/A snv 0.91 1
rs10195713 2 157664393 intergenic variant C/T snv 0.89 1
rs10241173 7 124813204 intergenic variant A/C;G snv 1
rs10428766 6 150052058 intergenic variant C/T snv 0.19 1
rs10471939 5 55180855 intergenic variant T/A snv 0.11 1
rs10473333 5 43866494 intergenic variant T/A snv 6.4E-02 1
rs10508366 10 8735729 intergenic variant C/T snv 0.20 1
rs10822220 10 63841301 intron variant A/G snv 0.17 1
rs11077961 17 83054873 upstream gene variant A/G;T snv 1
rs111526888 18 60304392 downstream gene variant A/C;G snv 1
rs11164971 1 91576688 regulatory region variant T/G snv 0.15 1
rs111678372 5 36087768 intergenic variant C/T snv 1.2E-02 1
rs11265402 1 160443300 regulatory region variant C/T snv 0.18 1
rs112711080 2 37335250 upstream gene variant C/T snv 5.2E-02 1
rs113252371 16 30465196 intergenic variant C/T snv 0.15 1
rs113317835 7 3088056 intron variant C/G;T snv 1
rs113844630 12 116899298 intergenic variant T/C snv 0.21 1
rs114422334 6 31263867 downstream gene variant C/G;T snv 1
rs114965247 6 31382526 upstream gene variant T/A;G snv 1
rs115039395 2 102545057 intergenic variant C/G snv 1.4E-02 1
rs115978073 2 213186248 intergenic variant T/C snv 5.1E-02 1
rs11658674 17 78245707 upstream gene variant T/C snv 0.20 1
rs116847786 22 28765016 intergenic variant G/A snv 4.6E-02 1
rs117072053 15 79975139 upstream gene variant C/T snv 2.0E-02 1