Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs199925463
rs199925463
RAD51
T 0.700 CausalMutation CLINVAR A novel DCC mutation and genetic heterogeneity in congenital mirror movements. 21242494

2011
dbSNP: rs34091239
rs34091239
RAD51
CA 0.700 CausalMutation CLINVAR A novel DCC mutation and genetic heterogeneity in congenital mirror movements. 21242494

2011
dbSNP: rs1555429623
rs1555429623
RAD51
A 0.700 CausalMutation CLINVAR