Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1567941252
rs1567941252
Entrez Id: 7703
Gene Symbol: PCGF2
PCGF2
CUI: C0685409
Disease:
Congenital Camptodactyly
A 0.700 GeneticVariation CLINVAR