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
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs780093 0.763 0.240 2 27519736 intron variant T/C snv 0.68 30
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
rs5182 0.742 0.160 3 148741608 synonymous variant C/T snv 0.49 0.41 16
rs5186 0.630 0.560 3 148742201 3 prime UTR variant A/C snv 0.23 0.21 38
rs995922697 0.724 0.560 3 49357413 missense variant A/G snv 4.1E-06 15
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs1042714 0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs41507953 0.790 0.280 8 27500988 missense variant A/G snv 8.7E-02 0.13 10
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs3834458 0.807 0.200 11 61827449 intron variant T/- del 0.28 7
rs662799 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 33
rs679620 0.716 0.360 11 102842889 missense variant T/C snv 0.58 0.57 17
rs200340021 0.925 0.080 12 14882204 missense variant C/T snv 7.0E-06 3