NOG, noggin, 9241

N. diseases: 206; N. variants: 17
Disease: Multiple synostoses syndrome 1 ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs387906844
rs387906844
Entrez Id: 9241
Gene Symbol: NOG
NOG
CUI: C0342282
Disease:
Multiple synostoses syndrome 1 		0.800 GeneticVariation UNIPROT Facioaudiosymphalangism syndrome and growth acceleration associated with a heterozygous NOG mutation. 20503332 2010
dbSNP: rs387906844
rs387906844
Entrez Id: 9241
Gene Symbol: NOG
NOG
CUI: C0342282
Disease:
Multiple synostoses syndrome 1 		0.800 GeneticVariation UNIPROT Heterozygous mutations in the gene encoding noggin affect human joint morphogenesis. 10080184 1999
dbSNP: rs387906844
rs387906844
Entrez Id: 9241
Gene Symbol: NOG
NOG
CUI: C0342282
Disease:
Multiple synostoses syndrome 1 		G 0.800 CausalMutation CLINVAR