Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
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
rs1801394 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
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
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs7412 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 47
rs964184 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs58542926 0.630 0.440 19 19268740 missense variant C/T snv 6.5E-02 5.8E-02 42
rs268
LPL
0.637 0.480 8 19956018 missense variant A/G snv 1.3E-02 1.3E-02 41
rs3856806 0.637 0.440 3 12434058 synonymous variant C/T snv 0.13 0.11 41
rs1799883 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 36
rs1800206 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 35
rs662799 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 33
rs11575937 0.653 0.480 1 156136985 missense variant G/A;T snv 29
rs3135506 0.708 0.400 11 116791691 missense variant G/A;C snv 3.0E-05; 6.8E-02 26
rs651821 0.851 0.360 11 116791863 5 prime UTR variant C/T snv 0.88 0.89 17
rs1800588 0.790 0.200 15 58431476 intron variant C/G;T snv 0.30 16
rs2075291 0.752 0.400 11 116790676 missense variant C/A;T snv 6.4E-03; 4.0E-06 15