Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs2275913 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs763780 0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 87
rs2228145 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 57
rs1143627 0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56 47
rs352140 0.630 0.680 3 52222681 synonymous variant C/A;G;T snv 2.0E-05; 0.49 42
rs3804099 0.627 0.680 4 153703504 synonymous variant T/C snv 0.40 0.48 40
rs3804100 0.633 0.720 4 153704257 synonymous variant T/C snv 9.0E-02 6.7E-02 36
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv 34
rs121917864 0.645 0.520 4 153704936 missense variant C/T snv 8.8E-05 9.8E-05 31
rs2297518 0.658 0.480 17 27769571 missense variant G/A snv 0.18 0.17 30
rs3748067 0.672 0.320 6 52190541 3 prime UTR variant C/T snv 6.2E-02 21
rs7804372 0.716 0.320 7 116554174 intron variant T/A snv 0.27 19
rs601338 0.742 0.280 19 48703417 stop gained G/A snv 0.38 0.45 19
rs5744168 0.701 0.480 1 223111858 stop gained G/A snv 5.3E-02 4.4E-02 18
rs3807987 0.732 0.280 7 116539780 intron variant G/A snv 7.6E-02 17
rs2066842 0.763 0.200 16 50710713 missense variant C/A;T snv 4.0E-06; 0.19 15