Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs7574865 0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs7975232
VDR
0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 56
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs2430561 0.590 0.760 12 68158742 intron variant T/A snv 0.36 50
rs187238 0.602 0.680 11 112164265 intron variant C/A;G snv 48
rs243865 0.600 0.640 16 55477894 intron variant C/T snv 0.19 48
rs1946518 0.602 0.760 11 112164735 intron variant T/G snv 0.60 46
rs755622 0.611 0.720 22 23894205 intron variant G/C snv 0.26 44
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21 38
rs187084 0.641 0.480 3 52227015 intron variant A/G snv 0.38 36
rs909253 0.641 0.600 6 31572536 intron variant A/G;T snv 34
rs2234767 0.649 0.280 10 88989499 intron variant G/A;T snv 0.15 30
rs1800890 0.658 0.400 1 206776020 intron variant A/T snv 0.32 29
rs2104286 0.662 0.440 10 6057082 intron variant T/C snv 0.18 25
rs57095329 0.677 0.480 5 160467840 intron variant A/G snv 7.8E-02 25
rs12212067 0.716 0.320 6 108659993 intron variant T/G snv 0.14 20
rs2187668 0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 20
rs2069705 0.695 0.440 12 68161231 intron variant G/A;C snv 19
rs706778 0.695 0.320 10 6056986 intron variant C/T snv 0.46 19
rs72928038 0.695 0.360 6 90267049 intron variant G/A snv 0.11 19
rs7517847 0.689 0.600 1 67215986 intron variant T/G snv 0.37 19