rs61752786

Orientation

minus

Stabilized

minus

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

Make rs61752786(A;A)

Make rs61752786(A;C)

Reference

GRCh38 38.1/142

Chromosome

8

Position

142875713

Gene

CYP11B1

is a	snp
is	mentioned by
dbSNP	rs61752786
dbSNP (classic)	rs61752786
ClinGen	rs61752786
ebi	rs61752786
HLI	rs61752786
Exac	rs61752786
Gnomad	rs61752786
Varsome	rs61752786
LitVar	rs61752786
Map	rs61752786
PheGenI	rs61752786
Biobank	rs61752786
1000 genomes	rs61752786
hgdp	rs61752786
ensembl	rs61752786
geneview	rs61752786
scholar	rs61752786
google	rs61752786
pharmgkb	rs61752786
gwascentral	rs61752786
openSNP	rs61752786
23andMe	rs61752786
SNPshot	rs61752786
SNPdbe	rs61752786
MSV3d	rs61752786
GWAS Ctlg	rs61752786

GMAF

0.007346

Max Magnitude

0

ClinVar
Risk	rs61752786(A;A) rs61752786(T;T)
Alt	rs61752786(A;A) rs61752786(T;T)
Reference	Rs61752786(C;C)
Significance	Other
Disease	Congenital adrenal hyperplasia Hyperaldosteronism not specified
Variation	info
Gene	CYP11B1
CLNDBN	Congenital adrenal hyperplasia Hyperaldosteronism, familial, type I not specified
Reversed	1
HGVS	NC_000008.10:g.143957129G>A; NC_000008.10:g.143957129G>T
CLNSRC	ClinVar LabCorp
CLNACC	RCV000029638.1, RCV000029637.2, RCV000397180.1, RCV000454869.1,