Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs63751068
rs63751068
PSEN1
0.810 GeneticVariation BEFREE The G183V mutation possibly causing Pick disease causes production of aberrant transcripts truncating the open reading frame after exon 5 sequence. 24101600

2014
dbSNP: rs63751068
rs63751068
PSEN1
0.810 GeneticVariation UNIPROT

dbSNP: rs63751068
rs63751068
PSEN1
T 0.810 CausalMutation CLINVAR