rs4670766
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in complete genomics |
Make rs4670766(C;C) |
Make rs4670766(C;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 37713399 |
is a | snp |
is | mentioned by |
dbSNP | rs4670766 |
dbSNP (classic) | rs4670766 |
ClinGen | rs4670766 |
ebi | rs4670766 |
HLI | rs4670766 |
Exac | rs4670766 |
Gnomad | rs4670766 |
Varsome | rs4670766 |
LitVar | rs4670766 |
Map | rs4670766 |
PheGenI | rs4670766 |
Biobank | rs4670766 |
1000 genomes | rs4670766 |
hgdp | rs4670766 |
ensembl | rs4670766 |
geneview | rs4670766 |
scholar | rs4670766 |
rs4670766 | |
pharmgkb | rs4670766 |
gwascentral | rs4670766 |
openSNP | rs4670766 |
23andMe | rs4670766 |
SNPshot | rs4670766 |
SNPdbe | rs4670766 |
MSV3d | rs4670766 |
GWAS Ctlg | rs4670766 |
GMAF | 0.1433 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 21116278] |
Trait | |
Title | Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease |
Risk Allele | |
P-val | 0.000002 |
Odds Ratio | 0.0053 [NR] unit decrease (interaction) |