Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10741657 0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 34
rs10759932 0.732 0.560 9 117702866 upstream gene variant T/C snv 0.18 15
rs11077 0.732 0.320 6 43523209 3 prime UTR variant T/G snv 0.47 14
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs11568820
VDR
0.672 0.480 12 47908762 intron variant C/T snv 0.38 27
rs12255372 0.667 0.480 10 113049143 intron variant G/A;T snv 28
rs12778366 0.724 0.480 10 67883321 upstream gene variant T/C;G snv 13
rs12785878 0.677 0.520 11 71456403 intron variant G/A;T snv 25
rs14035
RAN
0.742 0.320 12 130876696 3 prime UTR variant C/T snv 0.33 15
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs174537 0.708 0.400 11 61785208 non coding transcript exon variant G/T snv 0.28 23
rs174550 0.925 0.160 11 61804006 5 prime UTR variant T/C snv 0.28 13
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1800796 0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 74
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs1800872 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1801157 0.611 0.600 10 44372809 3 prime UTR variant C/T snv 0.16 46
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs1862513 0.763 0.360 19 7668907 upstream gene variant C/G;T snv 11
rs189037
ATM ; NPAT
0.689 0.400 11 108223106 5 prime UTR variant G/A snv 0.49 22
rs1927911 0.658 0.640 9 117707776 intron variant A/G snv 0.62 28
rs2016520 0.752 0.320 6 35411001 5 prime UTR variant C/T snv 0.78 16