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rs6410

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs6410(A;G)
Make rs6410(G;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position142879589
GeneCYP11B1
is asnp
is mentioned by
dbSNPrs6410
dbSNP (old)rs6410
ClinGenrs6410
ebirs6410
HLIrs6410
Exacrs6410
Gnomadrs6410
Varsomers6410
Maprs6410
PheGenIrs6410
Biobankrs6410
1000 genomesrs6410
hgdprs6410
ensemblrs6410
gopubmedrs6410
geneviewrs6410
scholarrs6410
googlers6410
pharmgkbrs6410
gwascentralrs6410
openSNPrs6410
23andMers6410
23andMe allrs6410
SNP Nexus

SNPshotrs6410
SNPdbers6410
MSV3drs6410
GWAS Ctlgrs6410
GMAF0.4229
Max Magnitude0
? (A;A) (A;G) (G;G) 28
[PMID 20708777] Association of DNA Polymorphisms Within the CYP11B2/CYP11B1 Locus and Postoperative Hypertension Risk in the Patients With Aldosterone-producing Adenomas


[PMID 20339375] Polymorphisms in CYP11B2 and CYP11B1 genes associated with primary hyperaldosteronism.


ClinVar
Risk rs6410(G;G)
Alt rs6410(G;G)
Reference Rs6410(A;A)
Significance Non-pathogenic
Disease Congenital adrenal hyperplasia Hyperaldosteronism
Variation info
Gene CYP11B1
CLNDBN Congenital adrenal hyperplasia Hyperaldosteronism, familial, type I
Reversed 1
HGVS NC_000008.10:g.143961005T>C
CLNSRC
CLNACC RCV000309802.1, RCV000396739.1,