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rs72556399

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs72556399(C;C)
Make rs72556399(C;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position66178643
GeneCRH
is asnp
is mentioned by
dbSNPrs72556399
ebirs72556399
HLIrs72556399
Exacrs72556399
Varsomers72556399
Maprs72556399
PheGenIrs72556399
hapmaprs72556399
1000 genomesrs72556399
hgdprs72556399
ensemblrs72556399
gopubmedrs72556399
geneviewrs72556399
scholarrs72556399
googlers72556399
pharmgkbrs72556399
gwascentralrs72556399
openSNPrs72556399
23andMers72556399
23andMe allrs72556399
SNP Nexus

SNPshotrs72556399
SNPdbers72556399
MSV3drs72556399
GWAS Ctlgrs72556399
Max Magnitude0
ClinVar
Risk rs72556399(C;C)
Alt rs72556399(C;C)
Reference rs72556399(G;G)
Significance Pathogenic
Disease ACTH deficiency
Variation info
Gene CRH
CLNDBN ACTH deficiency
Reversed 1
HGVS NC_000008.10:g.67090878C>G
CLNSRC GeneReviews
CLNACC RCV000033934.2,