rs61761208
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common/normal |
(A;T) | 8 | Early-onset Alzheimer's mutation (reported) |
Make rs61761208(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 1 |
Position | 226885602 |
Gene | PSEN2 |
is a | snp |
is | mentioned by |
dbSNP | rs61761208 |
dbSNP (classic) | rs61761208 |
ClinGen | rs61761208 |
ebi | rs61761208 |
HLI | rs61761208 |
Exac | rs61761208 |
Gnomad | rs61761208 |
Varsome | rs61761208 |
LitVar | rs61761208 |
Map | rs61761208 |
PheGenI | rs61761208 |
Biobank | rs61761208 |
1000 genomes | rs61761208 |
hgdp | rs61761208 |
ensembl | rs61761208 |
geneview | rs61761208 |
scholar | rs61761208 |
rs61761208 | |
pharmgkb | rs61761208 |
gwascentral | rs61761208 |
openSNP | rs61761208 |
23andMe | rs61761208 |
SNPshot | rs61761208 |
SNPdbe | rs61761208 |
MSV3d | rs61761208 |
GWAS Ctlg | rs61761208 |
Max Magnitude | 8 |
rs61761208, also known as c.421A>T, N141Y or Asn141Tyr, is a mutation in the presenilin 2 PSEN2 gene.
The minor allele is reported as pathogenic for early-onset Alzheimer's disease in the AlzForum database, based on a 2014 publication.[PMID 24838186]