Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs200340021 0.925 0.080 12 14882204 missense variant C/T snv 7.0E-06 3
rs281865545 0.695 0.360 17 64377836 missense variant C/G;T snv 18
rs3834458 0.807 0.200 11 61827449 intron variant T/- del 0.28 7
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs653178 0.672 0.600 12 111569952 intron variant C/T snv 0.67 41
rs662799 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 33
rs780093 0.763 0.240 2 27519736 intron variant T/C snv 0.68 30
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs911119 0.807 0.120 20 23632100 non coding transcript exon variant C/G;T snv 9
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49
rs995922697 0.724 0.560 3 49357413 missense variant A/G snv 4.1E-06 15
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
rs41507953 0.790 0.280 8 27500988 missense variant A/G snv 8.7E-02 0.13 10
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs5186 0.630 0.560 3 148742201 3 prime UTR variant A/C snv 0.23 0.21 38
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs708272 0.708 0.440 16 56962376 intron variant G/A snv 0.42 0.38 24
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249