Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 16
rs267734 0.925 0.120 1 150979001 upstream gene variant T/C snv 0.14 7
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 21
rs6834314 0.807 0.160 4 87292656 intergenic variant A/G snv 0.24 10
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs1229984 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs1693482 0.807 0.240 4 99342808 missense variant C/T snv 0.34 0.31 12
rs266729 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs2241766 0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48
rs1042713 0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs1042714 0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs1800888 0.695 0.400 5 148827322 missense variant C/T snv 9.1E-03 9.1E-03 23
rs4994 0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 65
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs4762
AGT
0.637 0.440 1 230710231 missense variant G/A snv 0.12 0.11 35
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs5186 0.630 0.560 3 148742201 3 prime UTR variant A/C snv 0.23 0.21 38
rs4918 0.763 0.400 3 186620593 missense variant G/A;C snv 0.67 12
rs1332629192
ALB
0.851 0.200 4 73404374 missense variant C/T snv 7
rs261332 0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80 20
rs1044250 0.807 0.240 19 8371280 missense variant C/T snv 0.30 0.29 12
rs3135506 0.708 0.400 11 116791691 missense variant G/A;C snv 3.0E-05; 6.8E-02 26
rs4420638 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43
rs5128 0.925 0.080 11 116832924 3 prime UTR variant G/C snv 0.84 0.87 8