Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs231775 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs28362491 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 56
rs3775291 0.602 0.640 4 186082920 missense variant C/G;T snv 1.2E-04; 0.28 51
rs1801274 0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 46
rs2066845 0.611 0.600 16 50722629 missense variant G/C;T snv 1.1E-02; 2.2E-04 46
rs3761548 0.620 0.680 X 49261784 intron variant G/A;T snv 42
rs10735810
VDR
0.662 0.640 12 47879112 start lost A/C;G;T snv 26
rs12785878 0.677 0.520 11 71456403 intron variant G/A;T snv 25
rs13266634 0.724 0.480 8 117172544 missense variant C/A;T snv 0.29 23
rs763361 0.689 0.520 18 69864406 missense variant T/A;C snv 4.0E-06; 0.52 21
rs555743307 0.695 0.440 16 27342243 missense variant G/A;T snv 3.6E-05; 2.9E-04 20
rs917997 0.701 0.480 2 102454108 downstream gene variant T/A;C snv 20
rs8192284 0.724 0.720 1 154454494 missense variant A/C;T snv 19
rs121908117 0.708 0.440 3 48466707 missense variant G/A snv 17
rs1378942
CSK
0.790 0.240 15 74785026 intron variant C/A;T snv 16
rs2229080
DCC
0.742 0.320 18 52906232 missense variant C/A;G snv 0.45 16
rs4246905 0.716 0.400 9 114790969 missense variant T/A;C snv 0.76 16
rs4810485 0.732 0.480 20 46119308 intron variant T/A;G snv 16
rs62324212 0.724 0.240 4 122639784 intron variant C/A;G snv 15
rs10988542 0.724 0.240 9 129894985 intron variant G/A;C snv 14
rs11145763 0.724 0.240 9 136369144 intron variant A/C;G;T snv 14