Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121909051
rs121909051
SERPINI1
0.800 GeneticVariation UNIPROT Mutant Neuroserpin (S49P) that causes familial encephalopathy with neuroserpin inclusion bodies is a poor proteinase inhibitor and readily forms polymers in vitro. 11880376

2002
dbSNP: rs121909051
rs121909051
SERPINI1
0.800 GeneticVariation UNIPROT Familial dementia caused by polymerization of mutant neuroserpin. 10517635

1999
dbSNP: rs121909051
rs121909051
SERPINI1
C 0.800 CausalMutation CLINVAR

dbSNP: rs121909052
rs121909052
SERPINI1
G 0.700 CausalMutation CLINVAR

dbSNP: rs121909053
rs121909053
SERPINI1
A 0.700 CausalMutation CLINVAR

dbSNP: rs121909054
rs121909054
SERPINI1
A 0.700 CausalMutation CLINVAR