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
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
rs142677199
ACE
0.882 0.040 17 63479897 missense variant G/A;T snv 3.2E-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
rs1042309696
ACE
17 63487006 synonymous variant T/C snv 2
rs4363
ACE
1.000 0.080 17 63497131 splice region variant G/A;C snv 0.52 2
rs1156835126
ACE
17 63477230 missense variant G/A snv 4.2E-05 1
rs4305
ACE
17 63480868 intron variant A/G snv 0.45 1
rs553520266
ACE
17 63479853 missense variant C/T snv 4.8E-05 2.1E-05 1
rs746566272
ACE
17 63484889 missense variant G/A snv 3.3E-05 7.0E-06 1
rs755506668
ACE
17 63496874 missense variant G/A;T snv 2.8E-05; 8.0E-06 1