Have questions? Visit https://www.reddit.com/r/SNPedia

rs11552588

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs11552588(A;G)
Make rs11552588(G;G)
ReferenceGRCh38 38.1/142
Chromosome1
Position147773279
GeneGJA5, LOC102723321
is asnp
is mentioned by
dbSNPrs11552588
dbSNP (classic)rs11552588
ClinGenrs11552588
ebirs11552588
HLIrs11552588
Exacrs11552588
Gnomadrs11552588
Varsomers11552588
LitVarrs11552588
Maprs11552588
PheGenIrs11552588
Biobankrs11552588
1000 genomesrs11552588
hgdprs11552588
ensemblrs11552588
geneviewrs11552588
scholarrs11552588
googlers11552588
pharmgkbrs11552588
gwascentralrs11552588
openSNPrs11552588
23andMers11552588
SNPshotrs11552588
SNPdbers11552588
MSV3drs11552588
GWAS Ctlgrs11552588
Max Magnitude0

[PMID 25992486] Two polymorphisms in the Cx40 promoter are associated with hypertension and left ventricular hypertrophy preferentially in men


ClinVar
Risk rs11552588(G;G)
Alt rs11552588(G;G)
Reference Rs11552588(A;A)
Significance Probable-non-pathogenic
Disease Familial atrial fibrillation
Variation info
Gene GJA5
CLNDBN Familial atrial fibrillation
Reversed 1
HGVS NC_000001.10:g.147245383T>C
CLNSRC
CLNACC RCV000330907.1,