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rs574125890

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common/normal
(G;T) 7 Alzheimer's disease (reported)
Make rs574125890(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position226888902
GenePSEN2
is asnp
is mentioned by
dbSNPrs574125890
dbSNP (classic)rs574125890
ClinGenrs574125890
ebirs574125890
HLIrs574125890
Exacrs574125890
Gnomadrs574125890
Varsomers574125890
LitVarrs574125890
Maprs574125890
PheGenIrs574125890
Biobankrs574125890
1000 genomesrs574125890
hgdprs574125890
ensemblrs574125890
geneviewrs574125890
scholarrs574125890
googlers574125890
pharmgkbrs574125890
gwascentralrs574125890
openSNPrs574125890
23andMers574125890
SNPshotrs574125890
SNPdbers574125890
MSV3drs574125890
GWAS Ctlgrs574125890
Max Magnitude7

rs574125890, also known as c.640G>T, V214L or Val214Leu, is a mutation in the presenilin 2 PSEN2 gene. Note the presence of another variant for this SNP, c.640G>A, of unknown pathogenicity.

The minor allele is reported as pathogenic for Alzheimer's disease in the AlzForum database, based on two publications,

including [PMID 24885952OA-icon.png].