Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs2234693 0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs9340799 0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs1800497 0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1801394 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs1803274 0.763 0.360 3 165773492 missense variant C/T snv 0.18 0.18 13
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs2032582 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs2230806 0.689 0.280 9 104858586 missense variant C/T snv 0.32 0.39 24
rs2236225 0.614 0.640 14 64442127 missense variant G/A snv 0.44 0.38 52
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs3732378 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 48
rs3732379 0.637 0.680 3 39265765 missense variant C/T snv 0.22 0.22 38
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs429358 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 66
rs4588
GC
0.597 0.720 4 71752606 missense variant G/A;T snv 1.6E-05; 0.25 53
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249