Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs10735810
VDR
0.662 0.640 12 47879112 start lost A/C;G;T snv 26
rs10931936 0.827 0.120 2 201279205 intron variant T/C snv 0.72 6
rs11225395 0.776 0.360 11 102725749 intron variant A/C;G snv 11
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs1136410 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs11571833 0.608 0.360 13 32398489 stop gained A/T snv 6.6E-03 6.0E-03 43
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
rs121912654 0.683 0.400 17 7675143 missense variant C/A;T snv 4.0E-05 21
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 101
rs121913343 0.611 0.520 17 7673803 missense variant G/A;C;T snv 1.2E-05 44
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144
rs13006529 0.851 0.080 2 201217736 missense variant T/A snv 0.41 0.42 7
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs1353702185 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 79
rs151322829 0.882 0.080 15 30905792 missense variant C/G;T snv 4.2E-03 5
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs16953002
FTO
0.882 0.080 16 54080912 intron variant G/A snv 0.19 5
rs17577 0.649 0.520 20 46014472 missense variant G/A;C snv 0.16 31
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