rs3097

minus

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

Make rs3097(A;A)

Make rs3097(A;G)

Reference

GRCh38 38.1/141

Chromosome

8

Position

142911899

Gene

CYP11B2

is a	snp
is	mentioned by
dbSNP	rs3097
dbSNP (classic)	rs3097
ClinGen	rs3097
ebi	rs3097
HLI	rs3097
Exac	rs3097
Gnomad	rs3097
Varsome	rs3097
LitVar	rs3097
Map	rs3097
PheGenI	rs3097
Biobank	rs3097
1000 genomes	rs3097
hgdp	rs3097
ensembl	rs3097
geneview	rs3097
scholar	rs3097
google	rs3097
pharmgkb	rs3097
gwascentral	rs3097
openSNP	rs3097
23andMe	rs3097
SNPshot	rs3097
SNPdbe	rs3097
MSV3d	rs3097
GWAS Ctlg	rs3097

GMAF

0.1405

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	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,