Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs863224494
rs863224494
L1CAM
A 0.700 CausalMutation CLINVAR Genetic and clinical aspects of X-linked hydrocephalus (L1 disease): Mutations in the L1CAM gene. 11438988

2001
dbSNP: rs863224494
rs863224494
L1CAM
A 0.700 CausalMutation CLINVAR Spectrum and detection rate of L1CAM mutations in isolated and familial cases with clinically suspected L1-disease. 10797421

2000