rs2298813
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs2298813(A;A) |
Make rs2298813(A;G) |
Make rs2298813(G;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 11 |
Position | 121522975 |
Gene | SORL1 |
is a | snp |
is | mentioned by |
dbSNP | rs2298813 |
dbSNP (classic) | rs2298813 |
ClinGen | rs2298813 |
ebi | rs2298813 |
HLI | rs2298813 |
Exac | rs2298813 |
Gnomad | rs2298813 |
Varsome | rs2298813 |
LitVar | rs2298813 |
Map | rs2298813 |
PheGenI | rs2298813 |
Biobank | rs2298813 |
1000 genomes | rs2298813 |
hgdp | rs2298813 |
ensembl | rs2298813 |
geneview | rs2298813 |
scholar | rs2298813 |
rs2298813 | |
pharmgkb | rs2298813 |
gwascentral | rs2298813 |
openSNP | rs2298813 |
23andMe | rs2298813 |
SNPshot | rs2298813 |
SNPdbe | rs2298813 |
MSV3d | rs2298813 |
GWAS Ctlg | rs2298813 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 25382023] Coding mutations in SORL1 and Alzheimer's disease
[PMID 24938503] Association of SORL1 gene variants with hippocampal and cerebral atrophy and Alzheimer's disease