rs72554626

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(A;A)	0	common in clinvar
(T;T)	0	common in complete genomics

Make rs72554626(A;G)

Make rs72554626(G;G)

Reference

GRCh38 38.1/141

Chromosome

8

Position

142912000

Gene

CYP11B2

is a	snp
is	mentioned by
dbSNP	rs72554626
dbSNP (classic)	rs72554626
ClinGen	rs72554626
ebi	rs72554626
HLI	rs72554626
Exac	rs72554626
Gnomad	rs72554626
Varsome	rs72554626
LitVar	rs72554626
Map	rs72554626
PheGenI	rs72554626
Biobank	rs72554626
1000 genomes	rs72554626
hgdp	rs72554626
ensembl	rs72554626
geneview	rs72554626
scholar	rs72554626
google	rs72554626
pharmgkb	rs72554626
gwascentral	rs72554626
openSNP	rs72554626
23andMe	rs72554626
SNPshot	rs72554626
SNPdbe	rs72554626
MSV3d	rs72554626
GWAS Ctlg	rs72554626

Max Magnitude

0

OMIM	124080
Desc
Variant	0012
Related	also

ClinVar
Risk	rs72554626(G;G)
Alt	rs72554626(G;G)
Reference	Rs72554626(A;A)
Significance	Pathogenic
Disease	Corticosterone methyloxidase type 2 deficiency
Variation	info
Gene	CYP11B2
CLNDBN	Corticosterone methyloxidase type 2 deficiency
Reversed	1
HGVS	NC_000008.10:g.143993416T>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000018381.27,