Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121909497 0.925 0.080 11 102955390 missense variant A/G snv 3
rs137854438 1.000 0.080 8 143728570 stop gained A/T snv 2
rs79204362 0.763 0.120 2 38071251 missense variant C/T snv 5.8E-03 1.7E-03 10
rs368705607 0.882 0.120 1 226225766 missense variant T/C;G snv 2.8E-05; 4.0E-06 7
rs104894378 0.882 0.120 12 114385521 missense variant C/G;T snv 6
rs104894381 0.925 0.120 12 114401830 missense variant C/T snv 5
rs121918502 0.790 0.160 10 121517351 missense variant G/C snv 9
rs1057519320 0.807 0.160 15 48444574 missense variant G/A snv 7
rs1057519321 0.807 0.160 5 128349391 missense variant C/A;T snv 7
rs57865060 0.827 0.160 2 38074704 missense variant C/T snv 1.1E-02 5.7E-03 6
rs104894232 0.925 0.160 11 125900000 missense variant A/G snv 1.1E-03 1.0E-03 4
rs28939086 0.925 0.160 7 107690220 missense variant A/C;G snv 2.0E-04; 4.0E-06 4
rs201968272 0.925 0.160 12 31089147 missense variant G/A snv 3
rs746147592 1.000 0.160 X 100665627 missense variant G/A;C snv 5.5E-06 2
rs786201044 0.827 0.200 10 87933165 missense variant T/C snv 8
rs12720071 0.807 0.200 6 88141462 3 prime UTR variant T/C snv 0.11 7
rs7650466 0.851 0.200 3 89481208 3 prime UTR variant C/T snv 0.23 7
rs121918214
FTO
1.000 0.200 16 53873837 missense variant G/A snv 4.0E-06 7.0E-06 3
rs745616565
FTO
1.000 0.200 16 53873855 missense variant G/A snv 1.6E-05 2.1E-05 3
rs781028867
FTO
1.000 0.200 16 53873846 missense variant C/A;T snv 4.0E-06 3
rs80338852 0.925 0.200 13 31317599 stop gained T/A;C snv 8.0E-06 3
rs121909173 0.851 0.240 3 57199901 missense variant C/G snv 2.8E-05 1.4E-05 5
rs121912974
POR
0.882 0.240 7 75983548 missense variant G/C snv 2.4E-04 2.2E-04 4
rs201405525 0.925 0.240 8 90044993 missense variant G/A;C snv 4.5E-04; 4.0E-06 3
rs806368 0.752 0.280 6 88140381 3 prime UTR variant T/C snv 0.19 14