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
rs4986790 0.465 0.750 9 117713024 missense variant A/G,T snp 6.1E-02; 4.0E-06 6.7E-02 146
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
rs1045642 0.520 0.714 7 87509329 synonymous variant A/G,T snp 0.50 0.56 108
rs1799782 0.523 0.607 19 43553422 stop gained G/A snp 9.5E-02 7.1E-02 84
rs1052133 0.533 0.643 3 9757089 missense variant C/G snp 0.27 0.22 77
rs1801282 0.543 0.679 3 12351626 missense variant C/G snp 0.11 1.0E-01 77
rs1805087
MTR
0.538 0.679 1 236885200 missense variant A/G snp 0.20 0.21 75
rs1805192 0.545 0.679 3 12379739 missense variant C/G snp 75
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
rs28934576 0.563 0.536 17 7673802 missense variant C/A,G,T snp 4.0E-06; 1.6E-05 64
rs1801394 0.577 0.643 5 7870860 missense variant A/G snp 0.47 0.46 60
rs7903146 0.596 0.536 10 112998590 intron variant C/G,T snp 0.26 59
rs121434592 0.582 0.500 14 104780214 missense variant C/T snp 4.0E-06 56
rs104886003 0.580 0.393 3 179218303 missense variant G/A,C snp 4.0E-06 52
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
rs1130409 0.590 0.500 14 20456995 missense variant T/A,C,G snp 4.0E-06; 4.0E-06; 0.42 0.44 45
rs121912651 0.618 0.464 17 7674221 missense variant G/A,C snp 4.0E-06 41
rs121913530 0.615 0.321 12 25245351 missense variant C/A,G,T snp 39
rs121913237 0.626 0.429 1 114716126 missense variant C/A,G,T snp 8.0E-06 37
rs2010963 0.630 0.607 6 43770613 5 prime UTR variant C/G snp 0.70 34
rs17879961 0.615 0.321 22 28725099 missense variant A/C,G snp 4.1E-03 1.1E-02 33