Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs113488022 0.407 0.786 7 140753336 missense variant snp 4.0E-06 267
rs397507444 0.457 0.714 1 11794407 missense variant T/G snp 169
rs25487 0.485 0.679 19 43551574 missense variant T/C snp 0.68 0.72 119
rs11540654 0.492 0.679 17 7676040 missense variant C/A,G,T snp 4.8E-05 3.2E-05 117
rs1695 0.510 0.679 11 67585218 missense variant A/G snp 0.34 0.35 100
rs13181 0.525 0.536 19 45351661 stop gained T/A,G snp 4.0E-06; 0.32 0.32 82
rs1052133 0.533 0.643 3 9757089 missense variant C/G snp 0.27 0.22 77
rs121913529 0.559 0.393 12 25245350 missense variant C/A,G,T snp 4.0E-06 70
rs121913279 0.559 0.536 3 179234297 missense variant A/G,T snp 4.0E-06; 4.0E-06 68
rs861539 0.561 0.464 14 103699416 missense variant G/A snp 0.29 0.29 60
rs1042522 0.563 0.643 17 7676154 stop gained G/C,T snp 0.67 0.62 56
rs121434592 0.582 0.500 14 104780214 missense variant C/T snp 4.0E-06 56
rs1799793 0.585 0.500 19 45364001 missense variant C/A,T snp 7.1E-06; 0.29 0.27 51
rs25489 0.587 0.571 19 43552260 stop lost C/G,T snp 8.5E-06; 7.1E-02 3.2E-05; 5.5E-02 48
rs1800566 0.605 0.571 16 69711242 missense variant G/A snp 0.25 0.21 41
rs17655 0.611 0.500 13 102875652 missense variant G/C snp 0.28 0.30 39
rs731236
VDR
0.605 0.571 12 47844974 synonymous variant A/G snp 0.33 0.33 39
rs113193886 0.608 0.464 7 143267671 missense variant A/T snp 4.0E-06 38
rs1544410
VDR
0.626 0.607 12 47846052 intron variant C/A,G,T snp 0.34 32
rs2228001
XPC
0.634 0.357 3 14145949 missense variant G/T snp 0.63 0.66 29
rs28934578 0.647 0.357 17 7675088 missense variant snp 4.0E-06 27
rs573154688 0.652 0.357 17 7670711 missense variant C/T snp 4.4E-05 3.2E-05 24
rs401681 0.679 0.464 5 1321972 intron variant C/T snp 0.48 22
rs2853669 0.724 0.179 5 1295234 TF binding site variant A/G snp 0.24 16
rs2853676 0.724 0.214 5 1288432 intron variant T/A,C snp 0.76 15