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rs672601309

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs672601309(G;G)
Make rs672601309(G;T)
ReferenceGRCh38.p2 38.2/144
Chromosome15
Position50490429
GeneUSP8
is asnp
is mentioned by
dbSNPrs672601309
ebirs672601309
HLIrs672601309
Exacrs672601309
Varsomers672601309
Maprs672601309
PheGenIrs672601309
hapmaprs672601309
1000 genomesrs672601309
hgdprs672601309
ensemblrs672601309
gopubmedrs672601309
geneviewrs672601309
scholarrs672601309
googlers672601309
pharmgkbrs672601309
gwascentralrs672601309
openSNPrs672601309
23andMers672601309
23andMe allrs672601309
SNP Nexus

SNPshotrs672601309
SNPdbers672601309
MSV3drs672601309
GWAS Ctlgrs672601309
Max Magnitude0
ClinVar
Risk rs672601309(G;G)
Alt rs672601309(G;G)
Reference rs672601309(T;T)
Significance Pathogenic
Disease Pituitary dependent hypercortisolism
Variation info
Gene USP8
CLNDBN Pituitary dependent hypercortisolism
Reversed 0
HGVS NC_000015.9:g.50782626T>G
CLNSRC
CLNACC RCV000149419.1,