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
rs104894230 0.564 0.600 11 534288 missense variant C/A;G;T snv 73
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1057519729 0.827 0.080 15 66435113 missense variant A/C snv 6
rs10735810
VDR
0.662 0.640 12 47879112 start lost A/C;G;T snv 26
rs112445441 0.658 0.400 12 25245347 missense variant C/A;G;T snv 32
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs1136410 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs1138272 0.611 0.600 11 67586108 missense variant C/T snv 5.9E-02 5.5E-02 42
rs11554290 0.583 0.600 1 114713908 missense variant T/A;C;G snv 59
rs121434569 0.581 0.520 7 55181378 missense variant C/T snv 2.8E-05 5.6E-05 70
rs121434592 0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs121913227 0.653 0.320 7 140753336 missense variant AC/CT;TT mnv 31
rs121913237 0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 50
rs121913240 0.672 0.440 12 25227342 missense variant T/A;C;G snv 24
rs121913250 0.683 0.440 1 114716127 missense variant C/A;G;T snv 25
rs121913255 0.667 0.400 1 114713907 missense variant T/A;G snv 26
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 101
rs121913338 0.677 0.400 7 140753354 missense variant T/A;C;G snv 24
rs121913348 0.763 0.480 7 140781617 missense variant C/A;G;T snv 20
rs121913351 0.776 0.240 7 140781611 missense variant C/A;G;T snv 4.0E-06 9
rs121913355 0.641 0.520 7 140781602 missense variant C/A;G;T snv 4.0E-06 42
rs121913357 0.742 0.320 7 140781603 stop gained C/A;G;T snv 12