Source: INFERRED ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs756522171
rs756522171
T 0.700 GeneticVariation CLINVAR Novel mutations in the CLN6 gene causing a variant late infantile neuronal ceroid lipofuscinosis. 12673792

2003

dbSNP: rs104894483
rs104894483
A 0.700 CausalMutation CLINVAR Mutations in a novel CLN6-encoded transmembrane protein cause variant neuronal ceroid lipofuscinosis in man and mouse. 11791207

2002