Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs4295
rs4295
ACE
2 17 63478937 intron variant C/G snv 0.61 0.700 1.000 1 2017 2017
dbSNP: rs4308
rs4308
ACE
1 17 63482264 intron variant A/G snv 0.71 0.700 1.000 1 2017 2017