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rs3097

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs3097(A;A)
Make rs3097(A;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position142911899
GeneCYP11B2
is asnp
is mentioned by
dbSNPrs3097
dbSNP (old)rs3097
ClinGenrs3097
ebirs3097
HLIrs3097
Exacrs3097
Gnomadrs3097
Varsomers3097
Maprs3097
PheGenIrs3097
Biobankrs3097
1000 genomesrs3097
hgdprs3097
ensemblrs3097
gopubmedrs3097
geneviewrs3097
scholarrs3097
googlers3097
pharmgkbrs3097
gwascentralrs3097
openSNPrs3097
23andMers3097
23andMe allrs3097
SNP Nexus

SNPshotrs3097
SNPdbers3097
MSV3drs3097
GWAS Ctlgrs3097
GMAF0.1405
Max Magnitude0
? (A;A) (A;G) (G;G) 28
[PMID 21127960] Haplotype-Based Case-Control Study of the Human CYP11B2 Gene and Essential Hypertension in Yi and Hani Minorities of China


[PMID 21269059] Association of the human CYP11B2 gene and essential hypertension in southwest Han Chinese population: a haplotype-based case-control study.


ClinVar
Risk rs3097(A;A)
Alt rs3097(A;A)
Reference Rs3097(G;G)
Significance Non-pathogenic
Disease Hyperaldosteronism Corticosterone methyloxidase type 2 deficiency Corticosterone methyloxidase type 1 deficiency
Variation info
Gene CYP11B2
CLNDBN Hyperaldosteronism, familial, type I Corticosterone methyloxidase type 2 deficiency Corticosterone methyloxidase type 1 deficiency
Reversed 1
HGVS NC_000008.10:g.143993315C>T
CLNSRC
CLNACC RCV000301190.1, RCV000356040.1, RCV000393363.1,