NEUROG3, neurogenin 3, 50674

N. diseases: 49; N. variants: 8
Disease: Diarrhea 4, Malabsorptive, Congenital ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121917837
rs121917837
Entrez Id: 50674;101929021
Gene Symbol: NEUROG3;LOC101929021
NEUROG3;LOC101929021
CUI: C1835888
Disease:
Diarrhea 4, Malabsorptive, Congenital 		0.800 GeneticVariation UNIPROT Mutant neurogenin-3 in congenital malabsorptive diarrhea. 16855267 2006
dbSNP: rs121917838
rs121917838
Entrez Id: 50674;101929021
Gene Symbol: NEUROG3;LOC101929021
NEUROG3;LOC101929021
CUI: C1835888
Disease:
Diarrhea 4, Malabsorptive, Congenital 		0.800 GeneticVariation UNIPROT Mutant neurogenin-3 in congenital malabsorptive diarrhea. 16855267 2006
dbSNP: rs121917837
rs121917837
Entrez Id: 50674;101929021
Gene Symbol: NEUROG3;LOC101929021
NEUROG3;LOC101929021
CUI: C1835888
Disease:
Diarrhea 4, Malabsorptive, Congenital 		T 0.800 CausalMutation CLINVAR
dbSNP: rs121917838
rs121917838
Entrez Id: 50674;101929021
Gene Symbol: NEUROG3;LOC101929021
NEUROG3;LOC101929021
CUI: C1835888
Disease:
Diarrhea 4, Malabsorptive, Congenital 		A 0.800 CausalMutation CLINVAR
dbSNP: rs1461650439
rs1461650439
Entrez Id: 50674;101929021
Gene Symbol: NEUROG3;LOC101929021
NEUROG3;LOC101929021
CUI: C1835888
Disease:
Diarrhea 4, Malabsorptive, Congenital 		T 0.700 CausalMutation CLINVAR