Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs762559980
rs762559980
LIPA
A 0.700 GeneticVariation CLINVAR Intragenic deletion as a novel type of mutation in Wolman disease. 21963785

2011
dbSNP: rs762559980
rs762559980
LIPA
A 0.700 CausalMutation CLINVAR