Gene: AMMECR1 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 9949
Gene Symbol: AMMECR1
AMMECR1 		0.400 Biomarker phenotype GENOMICS_ENGLAND AMMECR1: a single point mutation causes developmental delay, midface hypoplasia and elliptocytosis. 27811305 2017
Entrez Id: 9949
Gene Symbol: AMMECR1
AMMECR1 		0.400 CausalMutation phenotype CLINVAR
Entrez Id: 9949
Gene Symbol: AMMECR1
AMMECR1 		0.400 Biomarker phenotype HPO