Have questions? Visit https://www.reddit.com/r/SNPedia

rs672601307

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs672601307(C;C)
Make rs672601307(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome15
Position50490443
GeneUSP8
is asnp
is mentioned by
dbSNPrs672601307
ebirs672601307
HLIrs672601307
Exacrs672601307
Varsomers672601307
Maprs672601307
PheGenIrs672601307
hapmaprs672601307
1000 genomesrs672601307
hgdprs672601307
ensemblrs672601307
gopubmedrs672601307
geneviewrs672601307
scholarrs672601307
googlers672601307
pharmgkbrs672601307
gwascentralrs672601307
openSNPrs672601307
23andMers672601307
23andMe allrs672601307
SNP Nexus

SNPshotrs672601307
SNPdbers672601307
MSV3drs672601307
GWAS Ctlgrs672601307
Max Magnitude0
ClinVar
Risk rs672601307(C;C)
Alt rs672601307(C;C)
Reference rs672601307(T;T)
Significance Pathogenic
Disease Pituitary dependent hypercortisolism
Variation info
Gene USP8
CLNDBN Pituitary dependent hypercortisolism
Reversed 0
HGVS NC_000015.9:g.50782640T>C
CLNSRC
CLNACC RCV000149417.1,