Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1201229554
rs1201229554
LDLRAP1
T 0.700 CausalMutation CLINVAR Autosomal recessive hypercholesterolemia caused by mutations in a putative LDL receptor adaptor protein. 11326085

2001