Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10181656 0.763 0.360 2 191105153 intron variant G/C snv 0.79 1
rs10865331 0.827 0.120 2 62324337 intergenic variant A/G snv 0.57 5
rs11209026 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 5
rs114212579 1.000 0.080 6 31968280 non coding transcript exon variant G/T snv 1
rs114265779 1.000 0.080 6 30213844 upstream gene variant C/T snv 1
rs114383947 1.000 0.080 6 31010940 intron variant C/T snv 1
rs114598684 1.000 0.080 6 31413173 intron variant C/T snv 1
rs114757170 1.000 0.080 6 30618254 intron variant G/A snv 1
rs115112280 1.000 0.080 6 32390772 non coding transcript exon variant T/A;G snv 1
rs115145466 1.000 0.080 6 32251264 upstream gene variant C/A;T snv 1
rs115429782 1.000 0.080 6 31297975 intron variant T/C snv 1
rs115429849 1.000 0.080 6 30416827 intron variant G/A snv 1
rs115529844 1.000 0.080 6 29850244 non coding transcript exon variant C/T snv 1
rs115618145 1.000 0.080 6 30102498 upstream gene variant C/G snv 1
rs115645848 1.000 0.080 6 29622938 intron variant C/G;T snv 1
rs115872194 1.000 0.080 6 31639897 intron variant C/A;T snv 1
rs115928623 1.000 0.080 6 29971371 intron variant A/T snv 1
rs116199901 1.000 0.080 6 30315875 intron variant G/C snv 1
rs116340302 1.000 0.080 6 31528604 non coding transcript exon variant A/T snv 1
rs116805908 1.000 0.080 6 31173746 non coding transcript exon variant C/T snv 1
rs12044149 0.925 0.080 1 67135003 intron variant G/C;T snv 1
rs12188300 0.807 0.120 5 159402519 intron variant A/G;T snv 6
rs12191877 0.851 0.120 6 31285148 intron variant C/T snv 0.12 2
rs12356475 1.000 0.080 10 66001962 intron variant T/C snv 0.15 1
rs13017599 0.882 0.160 2 60937196 non coding transcript exon variant G/A snv 0.25 2