rs574125890
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common/normal |
(G;T) | 7 | Alzheimer's disease (reported) |
Make rs574125890(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 1 |
Position | 226888902 |
Gene | PSEN2 |
is a | snp |
is | mentioned by |
dbSNP | rs574125890 |
dbSNP (classic) | rs574125890 |
ClinGen | rs574125890 |
ebi | rs574125890 |
HLI | rs574125890 |
Exac | rs574125890 |
Gnomad | rs574125890 |
Varsome | rs574125890 |
LitVar | rs574125890 |
Map | rs574125890 |
PheGenI | rs574125890 |
Biobank | rs574125890 |
1000 genomes | rs574125890 |
hgdp | rs574125890 |
ensembl | rs574125890 |
geneview | rs574125890 |
scholar | rs574125890 |
rs574125890 | |
pharmgkb | rs574125890 |
gwascentral | rs574125890 |
openSNP | rs574125890 |
23andMe | rs574125890 |
SNPshot | rs574125890 |
SNPdbe | rs574125890 |
MSV3d | rs574125890 |
GWAS Ctlg | rs574125890 |
Max Magnitude | 7 |
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 24885952].