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rs5534

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs5534(A;G)
Make rs5534(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position148079934
GeneNR3C2
is asnp
is mentioned by
dbSNPrs5534
dbSNP (classic)rs5534
ClinGenrs5534
ebirs5534
HLIrs5534
Exacrs5534
Gnomadrs5534
Varsomers5534
LitVarrs5534
Maprs5534
PheGenIrs5534
Biobankrs5534
1000 genomesrs5534
hgdprs5534
ensemblrs5534
geneviewrs5534
scholarrs5534
googlers5534
pharmgkbrs5534
gwascentralrs5534
openSNPrs5534
23andMers5534
SNPshotrs5534
SNPdbers5534
MSV3drs5534
GWAS Ctlgrs5534
GMAF0.4412
Max Magnitude0
? (A;A) (A;G) (G;G) 28


[PMID 21677697] SNPs in MicroRNA Binding Sites in 3'-UTRs of RAAS Genes Influence Arterial Blood Pressure and Risk of Myocardial Infarction


[PMID 25714450] Depressed patients in remission show an interaction between variance in the mineralocorticoid receptor NR3C2 gene and childhood trauma on negative memory bias


ClinVar
Risk rs5534(G;G)
Alt rs5534(G;G)
Reference Rs5534(A;A)
Significance Non-pathogenic
Disease Pseudohypoaldosteronism
Variation info
Gene NR3C2
CLNDBN Pseudohypoaldosteronism, Type I, Dominant
Reversed 1
HGVS NC_000004.11:g.149001085T>C
CLNSRC
CLNACC RCV000298395.1,