GMNN, geminin DNA replication inhibitor, 51053

N. diseases: 153; N. variants: 3
Disease: Short palpebral fissure ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs864309487
rs864309487
Entrez Id: 51053
Gene Symbol: GMNN
GMNN
CUI: C0423112
Disease:
Short palpebral fissure 		A 0.700 CausalMutation CLINVAR De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome. 26637980 2015