Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs587777570 1.000 2 148947018 missense variant G/A snv 4
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
rs774753616 1.000 20 45419351 missense variant G/A snv 1.2E-05 1.4E-05 3
rs781028867
FTO
1.000 0.200 16 53873846 missense variant C/A;T snv 4.0E-06 3
rs137854438 1.000 0.080 8 143728570 stop gained A/T snv 2
rs746147592 1.000 0.160 X 100665627 missense variant G/A;C snv 5.5E-06 2
rs769269532 1.000 0.040 17 72124262 missense variant A/G snv 2.4E-05 1.4E-05 2
rs104894381 0.925 0.120 12 114401830 missense variant C/T snv 5
rs4954218 0.925 0.080 2 135045855 intron variant G/T snv 0.83 5
rs587777108 0.925 0.080 11 63646550 missense variant T/C snv 5
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
rs1057517786 0.925 0.400 3 167704889 stop gained G/A snv 3
rs121909497 0.925 0.080 11 102955390 missense variant A/G snv 3
rs201405525 0.925 0.240 8 90044993 missense variant G/A;C snv 4.5E-04; 4.0E-06 3
rs201968272 0.925 0.160 12 31089147 missense variant G/A snv 3
rs587777186 0.925 18 62146023 missense variant A/G;T snv 3
rs80338852 0.925 0.200 13 31317599 stop gained T/A;C snv 8.0E-06 3
rs869025322 0.925 0.040 4 88521653 missense variant A/G snv 3
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
rs527236031 0.882 0.080 20 45424323 missense variant C/T snv 1.6E-05 4.2E-05 5
rs756632799 0.882 0.080 20 45416579 stop gained G/T snv 1.6E-05 7.0E-06 5
rs121912974
POR
0.882 0.240 7 75983548 missense variant G/C snv 2.4E-04 2.2E-04 4