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
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
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
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
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
rs17879961 0.615 0.321 22 28725099 missense variant A/C,G snp 4.1E-03 1.1E-02 33
rs1501299 0.647 0.536 3 186853334 intron variant G/C,T snp 6.4E-05; 0.30 28
rs1045485 0.652 0.393 2 201284866 missense variant G/A,C,T snp 4.0E-06; 9.0E-02 3.2E-05; 9.8E-02 26
rs10741657 0.715 0.286 11 14893332 intergenic variant A/G snp 0.64 15
rs1042821 0.756 0.214 2 47783349 missense variant G/A,C snp 0.18; 8.6E-06 0.19 11
rs2282679
GC
0.744 0.286 4 71742666 intron variant T/G snp 0.22 11
rs751856545 0.846 0.107 1 22784767 missense variant C/A,T snp 8.0E-06; 4.0E-06 3.2E-05 6