Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs746397087
rs746397087
T 0.700 GeneticVariation CLINVAR CLN8 disease caused by large genomic deletions. 28116333

2017

dbSNP: rs746397087
rs746397087
T 0.700 GeneticVariation CLINVAR The neuronal ceroid lipofuscinosis CLN8 membrane protein is a resident of the endoplasmic reticulum. 10861296

2000