HOXB4, homeobox B4, 3214

N. diseases: 44; N. variants: 1
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3809783
rs3809783
Entrez Id: 3213;3214;404266;406902
Gene Symbol: HOXB3;HOXB4;HOXB-AS3;MIR10A
HOXB3;HOXB4;HOXB-AS3;MIR10A
CUI: C0276138
Disease:
Viral myocarditis 		0.010 GeneticVariation BEFREE We found the rare allele T of rs3809783 was accumulated in VM patients and related to VM significantly. 26439049 2015