MSX1, msh homeobox 1, 4487

N. diseases: 180; N. variants: 21
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104893850
rs104893850
Entrez Id: 4487
Gene Symbol: MSX1
MSX1
CUI: C3489529
Disease:
Tooth Agenesis, Familial
T 0.700 CausalMutation CLINVAR