Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10168049 1.000 0.040 2 121320830 intergenic variant A/G snv 0.16 1
rs10459221 1.000 0.040 12 49073211 upstream gene variant C/A;G snv 1
rs10513249 1.000 0.040 9 114541631 intergenic variant C/A;G snv 1
rs10878840 1.000 0.040 12 68487269 upstream gene variant G/A snv 0.62 1
rs11098403 0.925 0.040 4 117725752 intergenic variant A/G snv 0.25 1
rs11678288 1.000 0.040 2 65547553 intron variant T/A snv 0.53 1
rs116927879 1.000 0.040 7 45825128 downstream gene variant G/A snv 0.21 1
rs11709009 1.000 0.040 3 42473630 downstream gene variant G/A;C snv 1
rs11710433 1.000 0.040 3 5663365 intergenic variant C/G;T snv 1
rs11724116 1.000 0.040 4 161372886 intergenic variant C/T snv 0.12 1
rs12202969 1.000 0.040 6 98128347 intron variant G/A snv 0.39 1
rs12204181 1.000 0.040 6 98131605 intron variant T/C;G snv 1
rs12334475 1.000 0.040 8 142064186 intergenic variant C/T snv 6.7E-02 1
rs12553324 1.000 0.040 9 23347867 intron variant C/A;G snv 1
rs12833856 1.000 0.040 12 110824378 intergenic variant A/G snv 1.6E-02 1
rs12938916 1.000 0.040 17 57788926 intron variant G/A snv 5.4E-02 1
rs12998006 1.000 0.040 2 210804282 intergenic variant T/C snv 0.24 1
rs13003991 1.000 0.040 2 65545822 intron variant C/G snv 0.59 1
rs13411201 1.000 0.040 2 60680195 downstream gene variant C/A snv 0.17 1
rs142643109 1.000 0.040 17 62310560 intergenic variant T/G snv 1.0E-02 1
rs143577122 1.000 0.040 7 145943513 intergenic variant C/T snv 2.8E-02 1
rs1477143 1.000 0.040 17 55258467 intergenic variant T/G snv 0.76 1
rs1487441 1.000 0.040 6 98106018 intron variant G/A snv 0.39 1
rs1506223 1.000 0.040 18 64715948 intergenic variant A/G;T snv 0.76 1
rs1553656 1.000 0.040 3 36818214 downstream gene variant T/A;C snv 1