MSX2, msh homeobox 2, 4488

N. diseases: 135; N. variants: 7
Disease: PARIETAL FORAMINA ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104893895
rs104893895
Entrez Id: 4488
Gene Symbol: MSX2
MSX2
CUI: C1868598
Disease:
PARIETAL FORAMINA 		A 0.700 CausalMutation CLINVAR