RAD51, RAD51 recombinase, 5888

N. diseases: 363; N. variants: 16
Disease: Dysmorphic features ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1057519413
rs1057519413
Entrez Id: 5888
Gene Symbol: RAD51
RAD51
CUI: C0432072
Disease:
Dysmorphic features 		A 0.700 CausalMutation CLINVAR A Dominant Mutation in Human RAD51 Reveals Its Function in DNA Interstrand Crosslink Repair Independent of Homologous Recombination. 26253028 2015
dbSNP: rs1057519413
rs1057519413
Entrez Id: 5888
Gene Symbol: RAD51
RAD51
CUI: C0432072
Disease:
Dysmorphic features 		A 0.700 CausalMutation CLINVAR Congenital mirror movements: phenotypes associated with DCC and RAD51 mutations. 25813273 2015
dbSNP: rs1057519413
rs1057519413
Entrez Id: 5888
Gene Symbol: RAD51
RAD51
CUI: C0432072
Disease:
Dysmorphic features 		A 0.700 CausalMutation CLINVAR Congenital mirror movements: mutational analysis of RAD51 and DCC in 26 cases. 24808016 2014