Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1039659576
MTR
0.689 0.520 1 236803473 missense variant A/G snv 21
rs104893951 0.851 0.080 6 1610780 missense variant T/A;C snv 8.0E-06 5
rs104894232 0.925 0.160 11 125900000 missense variant A/G snv 1.1E-03 1.0E-03 4
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
rs1051740 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 56
rs1052108705 6 31165217 missense variant C/T snv 4.1E-06 2.1E-05 3
rs1057517786 0.925 0.400 3 167704889 stop gained G/A snv 3
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
rs1206736425 1 161626229 missense variant T/C snv 2
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs121909173 0.851 0.240 3 57199901 missense variant C/G snv 2.8E-05 1.4E-05 5
rs121909497 0.925 0.080 11 102955390 missense variant A/G snv 3
rs121912678 0.851 0.080 2 157774114 missense variant C/G;T snv 8
rs121912974
POR
0.882 0.240 7 75983548 missense variant G/C snv 2.4E-04 2.2E-04 4
rs121913483 0.649 0.560 4 1801841 missense variant C/A;G;T snv 4.2E-06; 1.3E-05 31
rs121913499 0.605 0.520 2 208248389 missense variant G/A;C;T snv 51
rs121918214
FTO
1.000 0.200 16 53873837 missense variant G/A snv 4.0E-06 7.0E-06 3
rs121918355 0.807 0.280 14 74555629 stop gained G/A;T snv 2.1E-05; 4.2E-06 7
rs121918502 0.790 0.160 10 121517351 missense variant G/C snv 9
rs12329305 2 19353152 synonymous variant C/A;T snv 1.6E-04; 5.5E-02 1
rs1234344050 2 188984825 missense variant C/G snv 4.0E-06 2
rs12720071 0.807 0.200 6 88141462 3 prime UTR variant T/C snv 0.11 7
rs1359880314 0.763 0.320 21 45534541 synonymous variant C/T snv 1.6E-05 2.8E-05 12