Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10735810
VDR
0.662 0.640 12 47879112 start lost A/C;G;T snv 26
rs1130214 0.742 0.280 14 104793397 5 prime UTR variant C/A snv 0.31 12
rs1143623 0.677 0.440 2 112838252 upstream gene variant C/G snv 0.24 29
rs11568820
VDR
0.672 0.480 12 47908762 intron variant C/T snv 0.38 27
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs2010963 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs3025039 0.576 0.720 6 43784799 3 prime UTR variant C/T snv 0.13 62
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49
rs1130409 0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs4588
GC
0.597 0.720 4 71752606 missense variant G/A;T snv 1.6E-05; 0.25 53
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
rs1138272 0.611 0.600 11 67586108 missense variant C/T snv 5.9E-02 5.5E-02 42
rs10079250 0.827 0.120 5 150070569 missense variant T/C snv 9.9E-02 8.6E-02 7
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs731236
VDR
0.542 0.760 12 47844974 synonymous variant A/G snv 0.33 0.34 81
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188