Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1250546 0.925 0.080 10 79272775 intron variant A/G snv 0.36 3
rs657555 0.925 0.080 18 12847137 intron variant C/A;T snv 4
rs1250544 0.882 0.080 10 79273128 intron variant G/A snv 0.32 3
rs181359 0.882 0.080 22 21574352 intron variant G/A snv 0.21 3
rs4780355 0.882 0.120 16 11254001 intron variant T/C;G snv 3
rs7849191 0.882 0.120 9 4988761 intron variant C/T snv 0.50 3
rs9988642 0.882 0.080 1 67260421 downstream gene variant T/C snv 0.13 3
rs12570088 0.851 0.160 10 58178575 intergenic variant A/G snv 4.1E-02 4
rs1001007 0.827 0.120 3 46387167 intron variant A/G;T snv 5
rs1004234 0.827 0.120 5 132421409 intron variant A/G;T snv 5
rs10510607 0.827 0.120 3 28244770 intron variant C/T snv 0.15 5
rs10743181 0.827 0.120 11 2208529 regulatory region variant A/G snv 0.77 5
rs10750899 0.827 0.120 11 58517478 intergenic variant G/A snv 0.95 5
rs10761648 0.827 0.120 10 62594503 intron variant C/T snv 0.20 5
rs10775412 0.827 0.120 17 27542007 intron variant A/C snv 0.30 5
rs10800314 0.827 0.120 1 161502999 upstream gene variant C/A snv 0.65 5
rs10865331 0.827 0.120 2 62324337 intergenic variant A/G snv 0.57 5
rs10870077 0.827 0.120 9 136369439 intron variant C/G snv 0.38 5
rs10889676 0.827 0.120 1 67256884 intron variant C/A;T snv 5
rs11098964 0.827 0.120 4 79966815 intron variant A/G;T snv 5
rs111305875 0.827 0.120 6 167098098 intron variant T/G snv 3.0E-02 5
rs11190133 0.827 0.120 10 99518968 intergenic variant C/T snv 0.26 5
rs11221322 0.827 0.120 11 128476898 intron variant T/C snv 0.13 5
rs11229555 0.827 0.120 11 58641214 intron variant G/T snv 0.21 7
rs11306716 0.827 0.120 2 203843041 intergenic variant T/-;TT delins 5