rs3772616, AGTR1

N. diseases: 2
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Atrial Fibrillation
CUI: C0004238
Disease: Atrial Fibrillation
584 0.925 0.120 3 148720404 intron variant C/T snv 0.35 0.010 1.000 1 2017 2017
Conn Syndrome
CUI: C1384514
Disease: Conn Syndrome
25 0.925 0.120 3 148720404 intron variant C/T snv 0.35 0.010 1.000 1 2015 2015