NOG, noggin, 9241

N. diseases: 206; N. variants: 17
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104894612
rs104894612
Entrez Id: 9241
Gene Symbol: NOG
NOG
CUI: C3714899
Disease:
SYMPHALANGISM, PROXIMAL, 1A 		0.800 GeneticVariation UNIPROT Identification of a novel NOG gene mutation (P35S) in an Italian family with symphalangism. 11857750 2002
dbSNP: rs121908948
rs121908948
Entrez Id: 9241
Gene Symbol: NOG
NOG
CUI: C3714899
Disease:
SYMPHALANGISM, PROXIMAL, 1A 		0.800 GeneticVariation UNIPROT Identification of a novel NOG gene mutation (P35S) in an Italian family with symphalangism. 11857750 2002
dbSNP: rs104894602
rs104894602
Entrez Id: 9241
Gene Symbol: NOG
NOG
CUI: C3714899
Disease:
SYMPHALANGISM, PROXIMAL, 1A 		0.800 GeneticVariation UNIPROT Mutations of the NOG gene in individuals with proximal symphalangism and multiple synostosis syndrome. 11846737 2001
dbSNP: rs104894608
rs104894608
Entrez Id: 9241
Gene Symbol: NOG
NOG
CUI: C3714899
Disease:
SYMPHALANGISM, PROXIMAL, 1A 		0.800 GeneticVariation UNIPROT Mutations of the NOG gene in individuals with proximal symphalangism and multiple synostosis syndrome. 11846737 2001
dbSNP: rs104894609
rs104894609
Entrez Id: 9241
Gene Symbol: NOG
NOG
CUI: C3714899
Disease:
SYMPHALANGISM, PROXIMAL, 1A 		0.800 GeneticVariation UNIPROT Mutations of the NOG gene in individuals with proximal symphalangism and multiple synostosis syndrome. 11846737 2001
dbSNP: rs104894611
rs104894611
Entrez Id: 9241
Gene Symbol: NOG
NOG
CUI: C3714899
Disease:
SYMPHALANGISM, PROXIMAL, 1A 		0.800 GeneticVariation UNIPROT Mutations of the NOG gene in individuals with proximal symphalangism and multiple synostosis syndrome. 11846737 2001
dbSNP: rs104894612
rs104894612
Entrez Id: 9241
Gene Symbol: NOG
NOG
CUI: C3714899
Disease:
SYMPHALANGISM, PROXIMAL, 1A 		0.800 GeneticVariation UNIPROT Mutations of the NOG gene in individuals with proximal symphalangism and multiple synostosis syndrome. 11846737 2001
dbSNP: rs121908948
rs121908948
Entrez Id: 9241
Gene Symbol: NOG
NOG
CUI: C3714899
Disease:
SYMPHALANGISM, PROXIMAL, 1A 		0.800 GeneticVariation UNIPROT Mutations of the NOG gene in individuals with proximal symphalangism and multiple synostosis syndrome. 11846737 2001
dbSNP: rs104894602
rs104894602
Entrez Id: 9241
Gene Symbol: NOG
NOG
CUI: C3714899
Disease:
SYMPHALANGISM, PROXIMAL, 1A 		0.800 GeneticVariation UNIPROT Heterozygous mutations in the gene encoding noggin affect human joint morphogenesis. 10080184 1999
dbSNP: rs104894603
rs104894603
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: rs104894608
rs104894608
Entrez Id: 9241
Gene Symbol: NOG
NOG
CUI: C3714899
Disease:
SYMPHALANGISM, PROXIMAL, 1A 		0.800 GeneticVariation UNIPROT Heterozygous mutations in the gene encoding noggin affect human joint morphogenesis. 10080184 1999
dbSNP: rs104894609
rs104894609
Entrez Id: 9241
Gene Symbol: NOG
NOG
CUI: C3714899
Disease:
SYMPHALANGISM, PROXIMAL, 1A 		0.800 GeneticVariation UNIPROT Heterozygous mutations in the gene encoding noggin affect human joint morphogenesis. 10080184 1999
dbSNP: rs104894611
rs104894611
Entrez Id: 9241
Gene Symbol: NOG
NOG
CUI: C3714899
Disease:
SYMPHALANGISM, PROXIMAL, 1A 		0.800 GeneticVariation UNIPROT Heterozygous mutations in the gene encoding noggin affect human joint morphogenesis. 10080184 1999
dbSNP: rs104894612
rs104894612
Entrez Id: 9241
Gene Symbol: NOG
NOG
CUI: C3714899
Disease:
SYMPHALANGISM, PROXIMAL, 1A 		0.800 GeneticVariation UNIPROT Heterozygous mutations in the gene encoding noggin affect human joint morphogenesis. 10080184 1999
dbSNP: rs121908948
rs121908948
Entrez Id: 9241
Gene Symbol: NOG
NOG
CUI: C3714899
Disease:
SYMPHALANGISM, PROXIMAL, 1A 		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 		0.800 GeneticVariation UNIPROT Heterozygous mutations in the gene encoding noggin affect human joint morphogenesis. 10080184 1999
dbSNP: rs104894602
rs104894602
Entrez Id: 9241
Gene Symbol: NOG
NOG
CUI: C3714899
Disease:
SYMPHALANGISM, PROXIMAL, 1A 		G 0.800 CausalMutation CLINVAR
dbSNP: rs104894602
rs104894602
Entrez Id: 9241
Gene Symbol: NOG
NOG
CUI: C1861305
Disease:
TARSAL-CARPAL COALITION SYNDROME 		G 0.800 CausalMutation CLINVAR
dbSNP: rs104894603
rs104894603
Entrez Id: 9241
Gene Symbol: NOG
NOG
CUI: C0342282
Disease:
Multiple synostoses syndrome 1 		G 0.800 CausalMutation CLINVAR
dbSNP: rs104894608
rs104894608
Entrez Id: 9241
Gene Symbol: NOG
NOG
CUI: C3714899
Disease:
SYMPHALANGISM, PROXIMAL, 1A 		T 0.800 CausalMutation CLINVAR
dbSNP: rs104894609
rs104894609
Entrez Id: 9241
Gene Symbol: NOG
NOG
CUI: C3714899
Disease:
SYMPHALANGISM, PROXIMAL, 1A 		T 0.800 CausalMutation CLINVAR
dbSNP: rs104894610
rs104894610
Entrez Id: 9241
Gene Symbol: NOG
NOG
CUI: C1861305
Disease:
TARSAL-CARPAL COALITION SYNDROME 		A 0.800 GeneticVariation CLINVAR
dbSNP: rs104894610
rs104894610
Entrez Id: 9241
Gene Symbol: NOG
NOG
CUI: C1861305
Disease:
TARSAL-CARPAL COALITION SYNDROME 		T 0.800 CausalMutation CLINVAR
dbSNP: rs104894611
rs104894611
Entrez Id: 9241
Gene Symbol: NOG
NOG
CUI: C1861305
Disease:
TARSAL-CARPAL COALITION SYNDROME 		G 0.800 CausalMutation CLINVAR
dbSNP: rs104894611
rs104894611
Entrez Id: 9241
Gene Symbol: NOG
NOG
CUI: C3714899
Disease:
SYMPHALANGISM, PROXIMAL, 1A 		G 0.800 CausalMutation CLINVAR