rs11767557
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs11767557(C;C) |
Make rs11767557(C;T) |
Make rs11767557(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 7 |
Position | 143412046 |
Gene | EPHA1-AS1 |
is a | snp |
is | mentioned by |
dbSNP | rs11767557 |
dbSNP (classic) | rs11767557 |
ClinGen | rs11767557 |
ebi | rs11767557 |
HLI | rs11767557 |
Exac | rs11767557 |
Gnomad | rs11767557 |
Varsome | rs11767557 |
LitVar | rs11767557 |
Map | rs11767557 |
PheGenI | rs11767557 |
Biobank | rs11767557 |
1000 genomes | rs11767557 |
hgdp | rs11767557 |
ensembl | rs11767557 |
geneview | rs11767557 |
scholar | rs11767557 |
rs11767557 | |
pharmgkb | rs11767557 |
gwascentral | rs11767557 |
openSNP | rs11767557 |
23andMe | rs11767557 |
SNPshot | rs11767557 |
SNPdbe | rs11767557 |
MSV3d | rs11767557 |
GWAS Ctlg | rs11767557 |
GMAF | 0.1878 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
Alzheimer's disease associated, based on large 2011 study 10.1038/ng.801
[PMID 21460841] Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease
[PMID 22005930] Genome-wide association study of Alzheimer's disease with psychotic symptoms.
[PMID 25189118] Late-onset Alzheimer's risk variants in memory decline, incident mild cognitive impairment, and Alzheimer's disease
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 7
- Has genotype
- Has population
- Uses doi
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip Affy GenomeWide 6
- On chip Ancestry v2
- On chip FTDNA2
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip 23andMe v5
- On chip Ancestry v2c
- On chip Ancestry v2d