NOG, noggin, 9241

N. diseases: 206; N. variants: 17
Disease: BRACHYDACTYLY, TYPE B2 (disorder) ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs28937580
rs28937580
Entrez Id: 9241
Gene Symbol: NOG
NOG
CUI: C1969652
Disease:
BRACHYDACTYLY, TYPE B2 (disorder) 		0.800 GeneticVariation UNIPROT A new subtype of brachydactyly type B caused by point mutations in the bone morphogenetic protein antagonist NOGGIN. 17668388 2007
dbSNP: rs28937580
rs28937580
Entrez Id: 9241
Gene Symbol: NOG
NOG
CUI: C1969652
Disease:
BRACHYDACTYLY, TYPE B2 (disorder) 		T 0.800 CausalMutation CLINVAR
dbSNP: rs28937580
rs28937580
Entrez Id: 9241
Gene Symbol: NOG
NOG
CUI: C1969652
Disease:
BRACHYDACTYLY, TYPE B2 (disorder) 		G 0.800 CausalMutation CLINVAR