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rs672601306

From SNPedia

Orientationplus
Geno Mag Summary
(CTC;CTC) 0 common in clinvar
Make rs672601306(-;-)
Make rs672601306(-;TCC)
Make rs672601306(TCC;TCC)
ReferenceGRCh38.p2 38.2/144
Chromosome15
Position50490446
GeneUSP8
is asnp
is mentioned by
dbSNPrs672601306
ebirs672601306
HLIrs672601306
Exacrs672601306
Varsomers672601306
Maprs672601306
PheGenIrs672601306
hapmaprs672601306
1000 genomesrs672601306
hgdprs672601306
ensemblrs672601306
gopubmedrs672601306
geneviewrs672601306
scholarrs672601306
googlers672601306
pharmgkbrs672601306
gwascentralrs672601306
openSNPrs672601306
23andMers672601306
23andMe allrs672601306
SNP Nexus

SNPshotrs672601306
SNPdbers672601306
MSV3drs672601306
GWAS Ctlgrs672601306
Max Magnitude0
ClinVar
Risk rs672601306(;)
Alt rs672601306(;)
Reference rs672601306(CTC;CTC)
Significance Pathogenic
Disease Pituitary dependent hypercortisolism
Variation info
Gene USP8
CLNDBN Pituitary dependent hypercortisolism
Reversed 0
HGVS NC_000015.9:g.50782643_50782645delTCC
CLNSRC
CLNACC RCV000149416.1,