DisGeNET - a database of gene-disease associations

Gene: RAD51C ×

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Gene

Disease

Variant

Source

Association Type

Semantic type

Protein Class

Disease Class

Type

Original DB

Consequence

DSI _g

DPI _g

pLI

EI _gda

EL _gda

Score _gda

PMID

PMID Year

AF_EXOME

Num. PMIDs

Num. SNPs_gda

AF_GENOME

Gene

Disease

Score _gda

Association Type

Original DB

Sentence supporting the association

PMID

PMID Year

Entrez Id:	5889
Gene Symbol:	RAD51C

RAD51C

CUI:	C4228778
Disease:	Abnormality of radial ray

Abnormality of radial ray

0.300

Biomarker

GENOMICS_ENGLAND

Expanding the FANCO/RAD51C associated phenotype: Cleft lip and palate and lobar holoprosencephaly, two rare findings in Fanconi anemia.

2018