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
rs25487 0.485 0.679 19 43551574 missense variant T/C snp 0.68 0.72 119
rs1799782 0.523 0.607 19 43553422 stop gained G/A snp 9.5E-02 7.1E-02 84
rs13181 0.525 0.536 19 45351661 stop gained T/A,G snp 4.0E-06; 0.32 0.32 82
rs4880 0.536 0.643 6 159692840 missense variant A/G snp 0.48 0.47 81
rs1052133 0.533 0.643 3 9757089 missense variant C/G snp 0.27 0.22 77
rs1805087
MTR
0.538 0.679 1 236885200 missense variant A/G snp 0.20 0.21 75
rs121913529 0.559 0.393 12 25245350 missense variant C/A,G,T snp 4.0E-06 70
rs1042522 0.563 0.643 17 7676154 stop gained G/C,T snp 0.67 0.62 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
rs121913530 0.615 0.321 12 25245351 missense variant C/A,G,T snp 39
rs11549465 0.662 0.357 14 61740839 missense variant C/T snp 8.8E-02 7.0E-02 27
rs759728549 0.679 0.214 17 7676223 stop lost T/C snp 8.0E-06 26
rs401681 0.679 0.464 5 1321972 intron variant C/T snp 0.48 22
rs11549467 0.734 0.250 14 61740857 missense variant G/A snp 8.9E-03 1.1E-02 14
rs9582036 0.821 0.214 13 28311271 intron variant C/A snp 0.59 5