Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10499194 0.752 0.400 6 137681500 intron variant C/T snv 0.24 10
rs13277113
BLK
0.695 0.520 8 11491677 intron variant G/A snv 0.25 18
rs204989 0.925 0.120 6 32194075 intron variant G/A snv 0.21 2
rs204991 0.882 0.200 6 32193589 intron variant T/C snv 0.21 3
rs3890733
VDR
0.882 0.120 12 47895590 intron variant C/T snv 0.27 3
rs4760648
VDR
0.851 0.200 12 47886882 intron variant C/A;G;T snv 4
rs755622 0.611 0.720 22 23894205 intron variant G/C snv 0.26 44
rs7574865 0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs7975232
VDR
0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 56
rs1057523354 0.763 0.480 13 110179387 missense variant C/A snv 13
rs1061622 0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22 33
rs1143679 0.732 0.520 16 31265490 missense variant G/A snv 9.7E-02 0.11 14
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1477353313
ACR
0.925 0.120 22 50744085 missense variant T/G snv 2
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs2230926 0.662 0.440 6 137874929 missense variant T/C;G snv 4.0E-06; 5.4E-02 27
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs2501432 0.716 0.480 1 23875430 missense variant T/C;G snv 0.62 16
rs35761398 0.701 0.520 1 23875429 missense variant TT/CC mnv 19
rs3743930 0.611 0.720 16 3254626 missense variant C/G;T snv 7.1E-02 43
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
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182