Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs1800566 0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21 59
rs2228145 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 57
rs1801274 0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 46
rs3087243 0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 44
rs1258159645 0.630 0.600 16 69711128 missense variant G/A snv 7.0E-06 37
rs1884444 0.637 0.600 1 67168129 missense variant G/T snv 0.52 0.51 34
rs2043211 0.653 0.480 19 48234449 missense variant A/T snv 0.33 0.29 29
rs11547328 0.701 0.360 12 57751648 missense variant G/A;T snv 4.0E-06 27
rs3134603 0.851 0.360 6 32158225 non coding transcript exon variant A/C;G;T snv 4