Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10051330 5 158392616 intron variant A/G;T snv 2
rs10092965 8 8515975 intergenic variant A/G snv 0.43 2
rs10184428 2 164155317 intron variant C/A;G snv 5
rs10255839 7 27249498 intron variant G/A snv 0.87 6
rs10750766 11 65706327 regulatory region variant C/A snv 0.60 4
rs10897164 11 61510303 3 prime UTR variant A/G snv 0.13 3
rs11065979 0.851 0.200 12 111621753 intergenic variant C/T snv 0.30 12
rs11066280 0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 27
rs11099097 4 80246155 intergenic variant C/T snv 0.30 6
rs11105352 12 89632685 intron variant G/A snv 0.14 4
rs111478946 12 89665065 intron variant G/A snv 0.14 4
rs112640876 11 1873813 intron variant A/G;T snv 3
rs11513729 1.000 0.080 12 111835695 downstream gene variant C/T snv 0.29 5
rs11725969 4 155705436 intron variant C/T snv 0.24 5
rs11731886 4 155738667 downstream gene variant A/C snv 0.21 3
rs11781008 8 9295729 intron variant G/C;T snv 2
rs12050759 15 74972850 intron variant G/A snv 0.27 2
rs12080886 1 243222734 intron variant T/A;C snv 2
rs12118370 1 112605645 intron variant A/G snv 0.24 3
rs12194642 6 78829074 intergenic variant G/A snv 0.32 2
rs12509595 1.000 0.080 4 80261400 intergenic variant T/C snv 0.23 10
rs12579302 0.851 0.120 12 89656726 intron variant A/G snv 0.15 19
rs1275984 2 26688641 upstream gene variant A/C;G snv 4
rs1275985 2 26688877 upstream gene variant C/T snv 0.50 3
rs12799126 11 16286917 intron variant G/T snv 0.17 3