PCGF2, polycomb group ring finger 2, 7703

N. diseases: 114; N. variants: 1
Disease: Congenital Camptodactyly ×
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1567941252
rs1567941252 		0.807 0.240 17 38739601 missense variant G/A snv
CUI: C0685409
Disease: Congenital Camptodactyly
Congenital Camptodactyly 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases 0.700 0