Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs1799752
ACE
0.677 0.480 17 63488529 intron variant -/TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT delins 25
rs4291
ACE
0.724 0.400 17 63476833 upstream gene variant T/A;C snv 20
rs4343
ACE
0.742 0.480 17 63488670 synonymous variant G/A snv 0.53 14
rs4362
ACE
0.807 0.240 17 63496400 missense variant T/C;G snv 0.52; 1.2E-05 0.51 9
rs1415088003
ACE
0.827 0.160 17 63489038 synonymous variant C/T snv 4.0E-06 7
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
rs769397961
ACE
0.882 0.120 17 63488758 missense variant G/A snv 1.2E-05 3.5E-05 4
rs867394500
ACE
0.851 0.080 17 63477301 missense variant G/T snv 4
rs4309
ACE
0.925 0.120 17 63482562 synonymous variant C/T snv 0.46 0.36 3
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
rs767425642
ACE
0.882 0.120 17 63489010 missense variant G/A;T snv 3.2E-05; 4.0E-06 3
rs1042309696
ACE
17 63487006 synonymous variant T/C snv 2
rs121912703
ACE
17 63496977 missense variant C/T snv 3.7E-05 4.9E-05 2
rs1277204441
ACE
0.925 0.080 17 63479775 missense variant C/T snv 7.0E-06 2
rs1334067073
ACE
0.925 0.120 17 63478025 missense variant C/G;T snv 4.2E-06 2
rs1455404812
ACE
1.000 0.080 17 63488732 missense variant C/T snv 2