Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs11543848 0.790 0.240 7 55161562 missense variant G/A;C;T snv 7
rs1222213359 0.574 0.720 6 43770966 missense variant G/A snv 62
rs12901682 0.851 0.200 15 78540881 5 prime UTR variant A/C;T snv 4
rs1353702185 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 79
rs1412125 0.724 0.360 13 30467458 intron variant C/G;T snv 17
rs1535045 0.742 0.360 20 46119460 intron variant C/A;G;T snv 12
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs217727 0.641 0.480 11 1995678 non coding transcript exon variant G/A snv 0.20 34
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs2231142 0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 56
rs2249825 0.695 0.440 13 30463766 5 prime UTR variant G/A;C;T snv 23
rs25489 0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 78
rs28362491 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 56
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs699947 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs969129 0.851 0.200 5 35861166 intron variant T/A;G snv 4
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs746702110 0.627 0.480 3 9756778 missense variant C/T snv 1.2E-05 2.8E-05 38
rs140693 0.763 0.280 3 129436608 missense variant C/T snv 5.8E-02 3.1E-02 10