Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799752
ACE
0.677 0.480 17 63488529 intron variant -/TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT delins 25
rs4311
ACE
0.882 0.200 17 63483402 intron variant T/C snv 0.60 3
rs4351
ACE
0.925 0.160 17 63492371 intron variant G/A snv 0.50 3
rs4295
ACE
17 63478937 intron variant C/G snv 0.61 2
rs4329
ACE
17 63486097 intron variant A/C;G snv 2
rs4344
ACE
17 63489363 intron variant G/A;C snv 2
rs149155892
ACE
17 63498493 intron variant C/T snv 1.6E-02 1
rs4305
ACE
17 63480868 intron variant A/G snv 0.45 1
rs4308
ACE
17 63482264 intron variant A/G snv 0.71 1
rs9896208
ACE
17 63498748 intron variant T/C snv 0.57 1
rs121912704
ACE
1.000 0.120 17 63480479 stop gained C/A;G;T snv 2.0E-05; 4.0E-06 1
rs1341633213
ACE
1.000 0.120 17 63496422 stop gained C/T snv 4.0E-06 1
rs397514688
ACE
1.000 0.120 17 63483172 stop gained C/T snv 1.2E-05 2.8E-05 1
rs397514689
ACE
1.000 0.120 17 63488713 stop gained C/T snv 1.6E-05 1
rs980857256
ACE
1.000 0.080 17 63485015 stop gained C/T snv 8.2E-06 6.3E-05 1
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs4362
ACE
0.807 0.240 17 63496400 missense variant T/C;G snv 0.52; 1.2E-05 0.51 9
rs776943620
ACE
0.851 0.120 17 63477287 missense variant G/A snv 2.1E-05 7
rs1205538057
ACE
0.827 0.200 17 63483937 missense variant A/G snv 4.0E-06 5
rs1241356540
ACE
0.851 0.160 17 63497137 missense variant C/T snv 5
rs1401663578
ACE
0.882 0.120 17 63483037 missense variant A/G snv 1.4E-05 4
rs142677199
ACE
0.882 0.040 17 63479897 missense variant G/A;T snv 3.2E-05 4
rs143830698
ACE
0.882 0.120 17 63488659 missense variant G/A snv 8.4E-05 4
rs568401628
ACE
0.882 0.120 17 63497280 missense variant C/T snv 4.5E-05 7.0E-06 4
rs761401927
ACE
0.882 0.040 17 63488704 missense variant G/A snv 9.1E-05 4