Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs401681 0.620 0.640 5 1321972 intron variant C/T snv 0.48 36
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs104894230 0.564 0.600 11 534288 missense variant C/A;G;T snv 42
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 484
rs1136410 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs1138272 0.611 0.600 11 67586108 missense variant C/T snv 5.9E-02 5.5E-02 42
rs121434569 0.581 0.520 7 55181378 missense variant C/T snv 2.8E-05 5.6E-05 70
rs121434592 0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs121913227 0.653 0.320 7 140753336 missense variant AC/CT;TT mnv 31
rs121913355 0.641 0.520 7 140781602 missense variant C/A;G;T snv 4.0E-06 11
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 135
rs121913530 0.583 0.640 12 25245351 missense variant C/A;G;T snv 55
rs1353702185 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 79
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 187
rs17577 0.649 0.520 20 46014472 missense variant G/A;C snv 0.16 30
rs17655 0.597 0.560 13 102875652 missense variant G/C snv 0.28 0.30 52
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs1799793 0.557 0.640 19 45364001 missense variant C/A;T snv 7.1E-06; 0.29 72
rs1870377
KDR
0.695 0.520 4 55106807 missense variant T/A snv 0.22 0.20 25
rs2228001
XPC
0.570 0.480 3 14145949 missense variant G/T snv 0.63 0.65 60