Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1801274 0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 46
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs1990760 0.672 0.480 2 162267541 missense variant C/T snv 0.50 0.45 33
rs2032582 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs34536443 0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 25
rs35018800 0.790 0.160 19 10354167 missense variant G/A snv 4.6E-03 4.9E-03 9
rs4246905 0.716 0.400 9 114790969 missense variant T/A;C snv 0.76 16
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs5029941 1.000 0.080 6 137874923 missense variant C/T snv 1.2E-03 5.6E-03 2
rs5743708 0.525 0.800 4 153705165 missense variant G/A snv 1.7E-02 1.8E-02 98
rs721917 0.752 0.360 10 79946568 missense variant A/G snv 0.47 0.42 14
rs763780 0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 87
rs878859113 0.763 0.360 6 106971734 missense variant G/A snv 0.35 11
rs2305764 0.776 0.360 19 17203024 non coding transcript exon variant G/A snv 0.52 0.50 10
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1128503 0.564 0.760 7 87550285 synonymous variant A/G snv 0.54 0.63 64
rs352140 0.630 0.680 3 52222681 synonymous variant C/A;G;T snv 2.0E-05; 0.49 42
rs3810936 0.742 0.320 9 114790605 synonymous variant T/C snv 0.71 0.75 12
rs731236
VDR
0.542 0.760 12 47844974 synonymous variant A/G snv 0.33 0.34 81
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
rs10889677 0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 40