Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs28730839
ACE
17 63483140 missense variant C/A;G snv 4.0E-06; 4.8E-04 2
rs4329
ACE
17 63486097 intron variant A/C;G snv 2
rs4343
ACE
0.742 0.480 17 63488670 synonymous variant G/A snv 0.53 1
rs4351
ACE
0.925 0.160 17 63492371 intron variant G/A snv 0.50 1