rs4536

minus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs4536(A;A)

Make rs4536(A;G)

Reference

GRCh38 38.1/141

Chromosome

8

Position

142914345

Gene

CYP11B2

is a	snp
is	mentioned by
dbSNP	rs4536
dbSNP (classic)	rs4536
ClinGen	rs4536
ebi	rs4536
HLI	rs4536
Exac	rs4536
Gnomad	rs4536
Varsome	rs4536
LitVar	rs4536
Map	rs4536
PheGenI	rs4536
Biobank	rs4536
1000 genomes	rs4536
hgdp	rs4536
ensembl	rs4536
geneview	rs4536
scholar	rs4536
google	rs4536
pharmgkb	rs4536
gwascentral	rs4536
openSNP	rs4536
23andMe	rs4536
SNPshot	rs4536
SNPdbe	rs4536
MSV3d	rs4536
GWAS Ctlg	rs4536

GMAF

0.1648

Max Magnitude

0

?

(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	rs4536(A;A)
Alt	rs4536(A;A)
Reference	Rs4536(G;G)
Significance	Non-pathogenic
Disease	Hyperaldosteronism Corticosterone methyloxidase type 1 deficiency Corticosterone methyloxidase type 2 deficiency
Variation	info
Gene	CYP11B2
CLNDBN	Hyperaldosteronism, familial, type I Corticosterone methyloxidase type 1 deficiency Corticosterone methyloxidase type 2 deficiency
Reversed	1
HGVS	NC_000008.10:g.143995761C>T
CLNSRC
CLNACC	RCV000263084.1, RCV000315890.1, RCV000354330.1,