rs4935774
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs4935774(C;C) |
Make rs4935774(C;T) |
Make rs4935774(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 11 |
Position | 121451045 |
Gene | LOC105369536, SORL1 |
is a | snp |
is | mentioned by |
dbSNP | rs4935774 |
dbSNP (classic) | rs4935774 |
ClinGen | rs4935774 |
ebi | rs4935774 |
HLI | rs4935774 |
Exac | rs4935774 |
Gnomad | rs4935774 |
Varsome | rs4935774 |
LitVar | rs4935774 |
Map | rs4935774 |
PheGenI | rs4935774 |
Biobank | rs4935774 |
1000 genomes | rs4935774 |
hgdp | rs4935774 |
ensembl | rs4935774 |
geneview | rs4935774 |
scholar | rs4935774 |
rs4935774 | |
pharmgkb | rs4935774 |
gwascentral | rs4935774 |
openSNP | rs4935774 |
23andMe | rs4935774 |
SNPshot | rs4935774 |
SNPdbe | rs4935774 |
MSV3d | rs4935774 |
GWAS Ctlg | rs4935774 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 24938503] Association of SORL1 gene variants with hippocampal and cerebral atrophy and Alzheimer's disease