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
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
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
rs1048943 0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 88
rs738409 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 88
rs1137101 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs429358 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 66
rs4994 0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 65
rs11615 0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62
rs4149056 0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 45
rs268
LPL
0.637 0.480 8 19956018 missense variant A/G snv 1.3E-02 1.3E-02 41
rs3732379 0.637 0.680 3 39265765 missense variant C/T snv 0.22 0.22 38
rs1799883 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 36
rs4986938 0.641 0.600 14 64233098 3 prime UTR variant C/T snv 0.31 0.33 35
rs1800206 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 35
rs2066853
AHR
0.653 0.600 7 17339486 missense variant G/A snv 0.15 0.22 34
rs662799 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 33
rs174547 0.742 0.240 11 61803311 intron variant T/C snv 0.28 33
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 33
rs1256049 0.645 0.560 14 64257333 synonymous variant C/T snv 6.7E-02 6.3E-02 32
rs11575937 0.653 0.480 1 156136985 missense variant G/A;T snv 29
rs11066280 0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 27