Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4308
ACE
17 63482264 intron variant A/G snv 0.71 1
rs4292
ACE
1.000 0.040 17 63476980 upstream gene variant C/T snv 0.71 1
rs4295
ACE
17 63478937 intron variant C/G snv 0.61 2
rs4311
ACE
0.882 0.200 17 63483402 intron variant T/C snv 0.60 3
rs9896208
ACE
17 63498748 intron variant T/C snv 0.57 1
rs4362
ACE
0.807 0.240 17 63496400 missense variant T/C;G snv 0.52; 1.2E-05 0.51 9
rs4351
ACE
0.925 0.160 17 63492371 intron variant G/A snv 0.50 3
rs4331
ACE
1.000 0.040 17 63486691 synonymous variant A/G snv 0.50 0.46 1
rs4305
ACE
17 63480868 intron variant A/G snv 0.45 1
rs4293
ACE
17 63478305 non coding transcript exon variant G/A snv 0.45 1
rs4309
ACE
0.925 0.120 17 63482562 synonymous variant C/T snv 0.46 0.36 3
rs149155892
ACE
17 63498493 intron variant C/T snv 1.6E-02 1
rs4302
ACE
1.000 0.120 17 63480461 synonymous variant C/T snv 2.1E-03 8.2E-03 1
rs199591851
ACE
1.000 0.080 17 63481106 missense variant A/G snv 7.4E-04 6.8E-04 1
rs371131106
ACE
0.925 0.120 17 63485346 missense variant A/G snv 8.4E-05 1.6E-04 2
rs145579007
ACE
0.925 0.080 17 63496503 missense variant G/A snv 1.0E-04 1.0E-04 2
rs980857256
ACE
1.000 0.080 17 63485015 stop gained C/T snv 8.2E-06 6.3E-05 1
rs121912703
ACE
17 63496977 missense variant C/T snv 3.7E-05 4.9E-05 2
rs1156835126
ACE
17 63477230 missense variant G/A snv 4.2E-05 1
rs1330442011
ACE
1.000 0.080 17 63485024 missense variant A/G snv 1.6E-05; 4.1E-06 3.5E-05 1
rs769397961
ACE
0.882 0.120 17 63488758 missense variant G/A snv 1.2E-05 3.5E-05 4
rs1157043147
ACE
1.000 0.120 17 63477150 missense variant T/C snv 2.8E-05 1
rs397514688
ACE
1.000 0.120 17 63483172 stop gained C/T snv 1.2E-05 2.8E-05 1
rs776943620
ACE
0.851 0.120 17 63477287 missense variant G/A snv 2.1E-05 7
rs553520266
ACE
17 63479853 missense variant C/T snv 4.8E-05 2.1E-05 1