rs7571971
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs7571971(C;C) |
Make rs7571971(C;T) |
Make rs7571971(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 88595833 |
Gene | EIF2AK3 |
is a | snp |
is | mentioned by |
dbSNP | rs7571971 |
dbSNP (classic) | rs7571971 |
ClinGen | rs7571971 |
ebi | rs7571971 |
HLI | rs7571971 |
Exac | rs7571971 |
Gnomad | rs7571971 |
Varsome | rs7571971 |
LitVar | rs7571971 |
Map | rs7571971 |
PheGenI | rs7571971 |
Biobank | rs7571971 |
1000 genomes | rs7571971 |
hgdp | rs7571971 |
ensembl | rs7571971 |
geneview | rs7571971 |
scholar | rs7571971 |
rs7571971 | |
pharmgkb | rs7571971 |
gwascentral | rs7571971 |
openSNP | rs7571971 |
23andMe | rs7571971 |
SNPshot | rs7571971 |
SNPdbe | rs7571971 |
MSV3d | rs7571971 |
GWAS Ctlg | rs7571971 |
GMAF | 0.2874 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 21685912] |
Trait | |
Title | Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy. |
Risk Allele | |
P-val | 4E-13 |
Odds Ratio | 1.3300 [1.22-1.43] |
[PMID 23116876] An exploratory study on STX6, MOBP, MAPT, and EIF2AK3 and late-onset Alzheimer's disease.