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rs672601308

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs672601308(C;G)
Make rs672601308(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome15
Position50490444
GeneUSP8
is asnp
is mentioned by
dbSNPrs672601308
ebirs672601308
HLIrs672601308
Exacrs672601308
Varsomers672601308
Maprs672601308
PheGenIrs672601308
hapmaprs672601308
1000 genomesrs672601308
hgdprs672601308
ensemblrs672601308
gopubmedrs672601308
geneviewrs672601308
scholarrs672601308
googlers672601308
pharmgkbrs672601308
gwascentralrs672601308
openSNPrs672601308
23andMers672601308
23andMe allrs672601308
SNP Nexus

SNPshotrs672601308
SNPdbers672601308
MSV3drs672601308
GWAS Ctlgrs672601308
Max Magnitude0
ClinVar
Risk rs672601308(G;G)
Alt rs672601308(G;G)
Reference rs672601308(C;C)
Significance Pathogenic
Disease Pituitary dependent hypercortisolism
Variation info
Gene USP8
CLNDBN Pituitary dependent hypercortisolism
Reversed 0
HGVS NC_000015.9:g.50782641C>G
CLNSRC
CLNACC RCV000149418.1,