Gene: AGT ×
Source: ALL
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: rs2004776
rs2004776
AGT
5 1 230712956 intron variant C/G;T snv 0.700 1.000 2 2017 2018
dbSNP: rs2478539
rs2478539
AGT
1 1 230709026 intron variant G/T snv 0.57 0.700 1.000 1 2019 2019
dbSNP: rs2493134
rs2493134
AGT
4 1 230713613 intron variant T/C snv 0.57 0.700 1.000 1 2016 2016
dbSNP: rs699
rs699
AGT
134 0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 0.700 1.000 1 2019 2019