Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10988542 0.724 0.240 9 129894985 intron variant G/A;C snv 14
rs11145763 0.724 0.240 9 136369144 intron variant A/C;G;T snv 14
rs11580078 0.724 0.240 1 67203951 intron variant C/A;G snv 14
rs1332099 0.724 0.240 10 99538694 downstream gene variant T/C;G snv 14
rs2738774 0.724 0.240 20 63637985 downstream gene variant G/A;C snv 14
rs2807264 0.724 0.240 X 136583619 downstream gene variant C/A snv 14
rs4246905 0.716 0.400 9 114790969 missense variant T/A;C snv 0.76 15
rs4869313 0.724 0.240 5 96888176 intron variant T/A;G snv 14
rs55705316 0.724 0.240 1 206760172 regulatory region variant T/A;G snv 14
rs62324212 0.724 0.240 4 122639784 intron variant C/A;G snv 15
rs7660520 0.724 0.240 4 182824168 upstream gene variant G/A;C snv 14
rs7831697 0.724 0.240 8 137124061 regulatory region variant T/A;C;G snv 14
rs114846446 0.724 0.240 2 2944140 intron variant G/A snv 9.5E-03 14
rs117372389 0.724 0.240 16 50634166 3 prime UTR variant G/T snv 1.1E-02 14
rs17466626 0.724 0.240 12 40366829 non coding transcript exon variant A/G snv 1.7E-02 14
rs6679677 0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 25
rs11839053 0.724 0.240 13 106410694 intergenic variant T/C snv 7.0E-02 14
rs17885785 0.724 0.240 11 2146620 non coding transcript exon variant C/T snv 0.14 14
rs12863738 0.724 0.240 X 136949968 intron variant C/T snv 0.16 14
rs77150043 0.724 0.240 16 50270338 intron variant C/T snv 0.17 14
rs72743477 0.724 0.240 15 67171953 intron variant A/G snv 0.17 14
rs7672495 0.724 0.240 4 4990640 regulatory region variant T/C snv 0.21 14
rs2836882 0.724 0.240 21 39094644 intergenic variant G/A snv 0.23 15
rs1250563 0.724 0.240 10 79287626 intron variant G/C snv 0.24 14
rs1689510 0.724 0.240 12 56002984 non coding transcript exon variant G/C snv 0.25 16