NOG, noggin, 9241

N. diseases: 206; N. variants: 17
Disease: SYMPHALANGISM, PROXIMAL, 1A ×
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: C3714899
Disease:
SYMPHALANGISM, PROXIMAL, 1A 		T 0.810 CausalMutation CLINVAR
dbSNP: rs104894602
rs104894602
Entrez Id: 9241
Gene Symbol: NOG
NOG
CUI: C3714899
Disease:
SYMPHALANGISM, PROXIMAL, 1A 		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: rs104894611
rs104894611
Entrez Id: 9241
Gene Symbol: NOG
NOG
CUI: C3714899
Disease:
SYMPHALANGISM, PROXIMAL, 1A 		G 0.800 CausalMutation CLINVAR
dbSNP: rs104894612
rs104894612
Entrez Id: 9241
Gene Symbol: NOG
NOG
CUI: C3714899
Disease:
SYMPHALANGISM, PROXIMAL, 1A 		A 0.800 CausalMutation CLINVAR
dbSNP: rs121908948
rs121908948
Entrez Id: 9241
Gene Symbol: NOG
NOG
CUI: C3714899
Disease:
SYMPHALANGISM, PROXIMAL, 1A 		G 0.800 CausalMutation CLINVAR
dbSNP: rs104894613
rs104894613
Entrez Id: 9241
Gene Symbol: NOG
NOG
CUI: C3714899
Disease:
SYMPHALANGISM, PROXIMAL, 1A 		A 0.700 CausalMutation CLINVAR
dbSNP: rs1567745111
rs1567745111
Entrez Id: 9241
Gene Symbol: NOG
NOG
CUI: C3714899
Disease:
SYMPHALANGISM, PROXIMAL, 1A 		C 0.700 GeneticVariation CLINVAR
dbSNP: rs28937580
rs28937580
Entrez Id: 9241
Gene Symbol: NOG
NOG
CUI: C3714899
Disease:
SYMPHALANGISM, PROXIMAL, 1A 		0.810 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 		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: rs104894615
rs104894615
Entrez Id: 9241
Gene Symbol: NOG
NOG
CUI: C3714899
Disease:
SYMPHALANGISM, PROXIMAL, 1A 		0.700 GeneticVariation UNIPROT Heterozygous mutations in the gene encoding noggin affect human joint morphogenesis. 10080184 1999
dbSNP: rs28937580
rs28937580
Entrez Id: 9241
Gene Symbol: NOG
NOG
CUI: C3714899
Disease:
SYMPHALANGISM, PROXIMAL, 1A 		0.810 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 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: rs104894615
rs104894615
Entrez Id: 9241
Gene Symbol: NOG
NOG
CUI: C3714899
Disease:
SYMPHALANGISM, PROXIMAL, 1A 		0.700 GeneticVariation UNIPROT Mutations of the NOG gene in individuals with proximal symphalangism and multiple synostosis syndrome. 11846737 2001