Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1056836 0.581 0.680 2 38071060 missense variant G/C snv 0.51 58
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs121913530 0.583 0.640 12 25245351 missense variant C/A;G;T snv 63
rs1258159645 0.630 0.600 16 69711128 missense variant G/A snv 7.0E-06 37
rs1322648460 0.776 0.320 11 35139332 frameshift variant G/- delins 9
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs1859168 0.790 0.160 7 27202740 non coding transcript exon variant A/C;G;T snv 13
rs2075685 0.724 0.320 5 83076846 intron variant G/A;T snv 14
rs2736100 0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs36115365 0.807 0.160 5 1313127 upstream gene variant G/A;C;T snv 7
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs401681 0.620 0.640 5 1321972 intron variant C/T snv 0.48 42
rs4759314 0.649 0.440 12 53968051 non coding transcript exon variant G/A snv 0.93 31
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs8034191 0.695 0.440 15 78513681 intron variant T/C snv 0.27 24
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1800440 0.653 0.440 2 38070996 missense variant T/C;G snv 0.15; 4.0E-06 29
rs3218536 0.620 0.440 7 152648922 missense variant C/G;T snv 4.0E-06; 6.4E-02 37
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs121434592 0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144
rs1130409 0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72