Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1042713 0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs1800566 0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21 59
rs7975232
VDR
0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 56
rs1801275 0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36 58
rs11209026 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 46
rs1801274 0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 46
rs187238 0.602 0.680 11 112164265 intron variant C/A;G snv 48
rs1946518 0.602 0.760 11 112164735 intron variant T/G snv 0.60 46
rs2228145 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 57
rs3775291 0.602 0.640 4 186082920 missense variant C/G;T snv 1.2E-04; 0.28 51
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49
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
rs909253 0.641 0.600 6 31572536 intron variant A/G;T snv 34
rs4673 0.653 0.600 16 88646828 missense variant A/G;T snv 0.70 32
rs16139 0.658 0.560 7 24285260 missense variant T/A;C snv 4.0E-06; 3.0E-02 36
rs1800624 0.658 0.480 6 32184610 upstream gene variant A/G;T snv 33
rs1990760 0.672 0.480 2 162267541 missense variant C/T snv 0.50 0.45 33
rs653178 0.672 0.600 12 111569952 intron variant C/T snv 0.67 41
rs12232497 0.701 0.360 17 39883866 intergenic variant T/C snv 0.35 18
rs2187668 0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 20
rs917997 0.701 0.480 2 102454108 downstream gene variant T/A;C snv 20
rs12794714 0.708 0.360 11 14892029 synonymous variant G/A snv 0.41 0.35 15
rs2670660 0.708 0.400 17 5615686 intron variant A/G snv 0.41 15
rs12150220 0.724 0.360 17 5582047 missense variant A/T snv 0.37 0.33 14