Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs63751287
rs63751287
PSEN1
CUI: C0338656
Disease: Impaired cognition
Impaired cognition 		0.010 GeneticVariation BEFREE The second case had a PSEN1 M233V mutation with an earlier age of onset of 25 with cognitive decline, parkinsonism, and epilepsy. 30814350

2019