Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397507444 0.457 0.714 1 11794407 missense variant T/G snp 169
rs1799945 0.475 0.679 6 26090951 missense variant C/G snp 0.11 9.9E-02 152
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
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
rs9939609
FTO
0.580 0.607 16 53786615 intron variant T/A snp 0.42 74
rs7903146 0.596 0.536 10 112998590 intron variant C/G,T snp 0.26 59
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
rs1800566 0.605 0.571 16 69711242 missense variant G/A snp 0.25 0.21 41
rs17879961 0.615 0.321 22 28725099 missense variant A/C,G snp 4.1E-03 1.1E-02 33
rs532358159 0.634 0.536 16 69711143 missense variant G/A snp 4.0E-06 30
rs1501299 0.647 0.536 3 186853334 intron variant G/C,T snp 6.4E-05; 0.30 28
rs11549465 0.662 0.357 14 61740839 missense variant C/T snp 8.8E-02 7.0E-02 27
rs505922 0.724 0.357 None NA snp 0.37 24
rs11571833 0.652 0.250 13 32398489 stop gained A/T snp 6.6E-03 5.4E-03 23
rs397514495 0.707 0.286 17 7675070 missense variant C/A,T snp 1.2E-05 3.2E-05 22
rs486907 0.715 0.286 1 182585422 missense variant C/T snp 0.31 0.30 16
rs2066827 0.707 0.250 12 12718165 missense variant T/A,C,G snp 1.6E-04; 1.6E-05; 0.26 0.36 15