Disease: MYOFIBROMATOSIS, INFANTILE, 1 ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1060499542
rs1060499542
Entrez Id: 5159
Gene Symbol: PDGFRB
PDGFRB
CUI: C4551572
Disease:
MYOFIBROMATOSIS, INFANTILE, 1 		G 0.700 CausalMutation CLINVAR