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: rs699
rs699
AGT
134 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.100 0.795 39 1993 2014
dbSNP: rs4762
rs4762
AGT
35 0.637 0.440 1 230710231 missense variant G/A snv 0.12 0.11 0.090 0.667 9 1994 2015
dbSNP: rs2478544
rs2478544
AGT
1 1.000 0.040 1 230708450 intron variant C/A;G;T snv 0.010 1.000 1 2015 2015