Source: CLINVAR

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1555642784
rs1555642784
CNTNAP1
CUI: C0740279
Disease: Cerebellar atrophy
Cerebellar atrophy 		TC 0.700 CausalMutation CLINVAR

dbSNP: rs779027563
rs779027563
CNTNAP1
CUI: C0740279
Disease: Cerebellar atrophy
Cerebellar atrophy 		C 0.700 GeneticVariation CLINVAR Novel mutation in CNTNAP1 results in congenital hypomyelinating neuropathy. 27668699

2017