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

rs3802230

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs3802230(A;A)
Make rs3802230(A;C)
ReferenceGRCh38 38.1/141
Chromosome8
Position142911448
GeneCYP11B2
is asnp
is mentioned by
dbSNPrs3802230
dbSNP (old)rs3802230
ClinGenrs3802230
ebirs3802230
HLIrs3802230
Exacrs3802230
Gnomadrs3802230
Varsomers3802230
Maprs3802230
PheGenIrs3802230
Biobankrs3802230
1000 genomesrs3802230
hgdprs3802230
ensemblrs3802230
gopubmedrs3802230
geneviewrs3802230
scholarrs3802230
googlers3802230
pharmgkbrs3802230
gwascentralrs3802230
openSNPrs3802230
23andMers3802230
23andMe allrs3802230
SNP Nexus

SNPshotrs3802230
SNPdbers3802230
MSV3drs3802230
GWAS Ctlgrs3802230
GMAF0.4265
Max Magnitude0
? (A;A) (A;C) (C;C) 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 rs3802230(A;A)
Alt rs3802230(A;A)
Reference Rs3802230(C;C)
Significance Non-pathogenic
Disease Corticosterone methyloxidase type 2 deficiency Corticosterone methyloxidase type 1 deficiency Hyperaldosteronism
Variation info
Gene CYP11B2
CLNDBN Corticosterone methyloxidase type 2 deficiency Corticosterone methyloxidase type 1 deficiency Hyperaldosteronism, familial, type I
Reversed 0
HGVS NC_000008.10:g.143992864C>A
CLNSRC
CLNACC RCV000306434.1, RCV000346205.1, RCV000394920.1,