Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs231775 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs61752717 0.583 0.840 16 3243407 missense variant T/A;C snv 2.8E-04 72
rs699947 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs4588
GC
0.597 0.720 4 71752606 missense variant G/A;T snv 1.6E-05; 0.25 53
rs3775291 0.602 0.640 4 186082920 missense variant C/G;T snv 1.2E-04; 0.28 51
rs56149945 0.595 0.680 5 143399752 missense variant T/A;C snv 2.0E-02 49
rs3743930 0.611 0.720 16 3254626 missense variant C/G;T snv 7.1E-02 43
rs3761548 0.620 0.680 X 49261784 intron variant G/A;T snv 42
rs763059810 0.623 0.600 2 136115750 missense variant T/C snv 4.0E-06 41
rs1232898090 0.637 0.600 22 46198429 missense variant G/C;T snv 4.0E-06; 4.0E-06 40
rs855791 0.701 0.400 22 37066896 missense variant A/G;T snv 0.57; 4.0E-06 38
rs16139 0.658 0.560 7 24285260 missense variant T/A;C snv 4.0E-06; 3.0E-02 36
rs746682028 0.645 0.480 11 27658414 missense variant C/A;T snv 4.0E-06; 4.0E-06 36
rs909253 0.641 0.600 6 31572536 intron variant A/G;T snv 34
rs4950928 0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv 33