MSX1, msh homeobox 1, 4487

N. diseases: 180; N. variants: 21
Disease: Tooth Agenesis, Familial ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121913130
rs121913130
Entrez Id: 4487
Gene Symbol: MSX1
MSX1
CUI: C3489529
Disease:
Tooth Agenesis, Familial 		0.800 GeneticVariation UNIPROT The role of MSX1 in human tooth agenesis. 12097313 2002
dbSNP: rs121913130
rs121913130
Entrez Id: 4487
Gene Symbol: MSX1
MSX1
CUI: C3489529
Disease:
Tooth Agenesis, Familial 		0.800 GeneticVariation UNIPROT A human MSX1 homeodomain missense mutation causes selective tooth agenesis. 8696335 1996
dbSNP: rs121913130
rs121913130
Entrez Id: 4487
Gene Symbol: MSX1
MSX1
CUI: C3489529
Disease:
Tooth Agenesis, Familial 		A 0.800 CausalMutation CLINVAR