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
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs361525
TNF
0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 62
rs1800566 0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21 59
rs758272654 0.611 0.680 20 58909201 synonymous variant T/C snv 4.0E-06 7.0E-06 50
rs1051730 0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 43
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21 38
rs11547328 0.701 0.360 12 57751648 missense variant G/A;T snv 4.0E-06 27
rs752907384 0.827 0.200 6 43782077 missense variant C/G;T snv 8.0E-06 6