rs4298437
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 |
Make rs4298437(C;T) |
Make rs4298437(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 7 |
Position | 103985430 |
Gene | RELN |
is a | snp |
is | mentioned by |
dbSNP | rs4298437 |
dbSNP (classic) | rs4298437 |
ClinGen | rs4298437 |
ebi | rs4298437 |
HLI | rs4298437 |
Exac | rs4298437 |
Gnomad | rs4298437 |
Varsome | rs4298437 |
LitVar | rs4298437 |
Map | rs4298437 |
PheGenI | rs4298437 |
Biobank | rs4298437 |
1000 genomes | rs4298437 |
hgdp | rs4298437 |
ensembl | rs4298437 |
geneview | rs4298437 |
scholar | rs4298437 |
rs4298437 | |
pharmgkb | rs4298437 |
gwascentral | rs4298437 |
openSNP | rs4298437 |
23andMe | rs4298437 |
SNPshot | rs4298437 |
SNPdbe | rs4298437 |
MSV3d | rs4298437 |
GWAS Ctlg | rs4298437 |
GMAF | 0.2346 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 20452100] |
Trait | Alzheimer's disease |
Title | Alzheimer disease pathology in cognitively healthy elderly: A genome-wide study |
Risk Allele | |
P-val | 0.000002 |
Odds Ratio | None None |
The risk allele is T (in dbSNP orientation), according to a table published by the National Human Genome Research Institute.