Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 73
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 64
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 48
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 43
rs11540652 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 42
rs28934576 0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 39
rs104894230 0.564 0.600 11 534288 missense variant C/A;G;T snv 37
rs121913281 0.623 0.520 3 179234296 missense variant C/T snv 37
rs121912651 0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 37
rs121913482 0.630 0.680 4 1801837 missense variant C/T snv 35
rs104886003 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 35
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 34
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 31
rs4647924 0.600 0.520 4 1801844 missense variant C/A;G;T snv 4.2E-06; 4.2E-06 30
rs121913274 0.645 0.320 3 179218304 missense variant A/C;G;T snv 30
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 29
rs429358 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 29
rs1229984 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 27
rs7679673 0.677 0.440 4 105140377 intron variant C/A snv 0.50 25
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 25
rs11554290 0.583 0.600 1 114713908 missense variant T/A;C;G snv 25
rs121913273 0.605 0.440 3 179218294 missense variant G/A;C snv 25
rs28934575 0.641 0.400 17 7674230 missense variant C/A;G;T snv 25
rs1057519925 0.683 0.560 3 179210291 missense variant G/A;C snv 24
rs121913483 0.649 0.560 4 1801841 missense variant C/A;G;T snv 4.2E-06; 1.3E-05 23