HMX1, H6 family homeobox 1, 3166

N. diseases: 23; N. variants: 1
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs876657398
rs876657398
Entrez Id: 3166
Gene Symbol: HMX1
HMX1
CUI: C2677500
Disease:
Oculoauricular Syndrome 		G 0.700 CausalMutation CLINVAR