HOXB13, homeobox B13, 10481

N. diseases: 90; N. variants: 3
Disease: Neoplastic Syndromes, Hereditary ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs138213197
rs138213197
Entrez Id: 10481
Gene Symbol: HOXB13
HOXB13
CUI: C0027672
Disease:
Neoplastic Syndromes, Hereditary 		T 0.700 GeneticVariation CLINVAR Association between germline HOXB13 G84E mutation and risk of prostate cancer. 22781434 2012