Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs738409 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 88
rs12979860 0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs8099917 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 60
rs3775291 0.602 0.640 4 186082920 missense variant C/G;T snv 1.2E-04; 0.28 51
rs58542926 0.630 0.440 19 19268740 missense variant C/T snv 6.5E-02 5.8E-02 42
rs10741657 0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 34
rs4950928 0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv 33
rs1127354 0.667 0.400 20 3213196 missense variant C/A;G snv 7.5E-02 26
rs12980275 0.701 0.360 19 39241143 upstream gene variant A/G snv 0.36 23
rs3135932 0.677 0.480 11 117993348 missense variant A/G snv 0.13 0.11 23
rs12075 0.724 0.240 1 159205564 missense variant G/A snv 0.51 0.66 22
rs641738 0.689 0.320 19 54173068 missense variant T/A;C;G snv 22
rs2596542 0.724 0.200 6 31398818 upstream gene variant C/T snv 0.41 18
rs2287622 0.724 0.240 2 168973818 missense variant A/C;G;T snv 0.57 16
rs368234815 0.742 0.280 19 39248514 frameshift variant TT/G;T delins 15
rs179008 0.763 0.360 X 12885540 missense variant A/C;T snv 0.18 0.18 14
rs3747517 0.732 0.360 2 162272314 missense variant T/C snv 0.68 0.68 13
rs10846744 0.763 0.160 12 124827879 intron variant G/C snv 0.32 11
rs5888 0.752 0.200 12 124800202 synonymous variant A/G;T snv 0.59; 4.0E-06 11
rs3764880 0.752 0.320 X 12906707 start lost A/G snv 0.31 0.30 11
rs2229113 0.763 0.360 11 117998955 missense variant A/G snv 0.74 0.74 10