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
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs61752717 0.583 0.840 16 3243407 missense variant T/A;C snv 2.8E-04 72
rs3743930 0.611 0.720 16 3254626 missense variant C/G;T snv 7.1E-02 43
rs1800925 0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 37
rs2230926 0.662 0.440 6 137874929 missense variant T/C;G snv 4.0E-06; 5.4E-02 27
rs35761398 0.701 0.520 1 23875429 missense variant TT/CC mnv 19
rs28940580 0.742 0.560 16 3243447 missense variant C/A;G;T snv 1.0E-04; 8.0E-06 17
rs2501432 0.716 0.480 1 23875430 missense variant T/C;G snv 0.62 16
rs879761216 0.732 0.480 1 23875429 frameshift variant TT/C;T delins 14
rs1057523354 0.763 0.480 13 110179387 missense variant C/A snv 13
rs10036748 0.752 0.360 5 151078585 intron variant C/A;T snv 11
rs1194611372 0.763 0.320 1 152032679 missense variant A/C snv 9
rs3789604 0.776 0.360 1 113812320 synonymous variant T/A;C;G snv 8.5E-06; 1.3E-05; 0.17 9
rs1057519090 0.851 0.160 13 110492105 missense variant G/A snv 7
rs104895094 0.851 0.320 16 3243403 missense variant T/A;C snv 8.0E-06; 5.2E-03 5
rs2248098
VDR
0.925 0.120 12 47859573 intron variant A/G;T snv 4
rs4760648
VDR
0.851 0.200 12 47886882 intron variant C/A;G;T snv 4
rs741761 0.882 0.200 15 74411588 missense variant T/A;C snv 1.8E-04; 0.35 3
rs1385889785 1.000 0.040 1 157695436 missense variant G/C;T snv 4.0E-06; 4.0E-06 2
rs1477353313
ACR
0.925 0.120 22 50744085 missense variant T/G snv 2
rs2165667 0.925 0.040 4 186540475 intron variant A/G;T snv 2
rs7033979 0.925 0.040 9 92461698 intron variant A/G;T snv 2