rs476463
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs476463(A;A) |
Make rs476463(A;G) |
Make rs476463(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 33782463 |
Gene | CSMD2 |
is a | snp |
is | mentioned by |
dbSNP | rs476463 |
dbSNP (classic) | rs476463 |
ClinGen | rs476463 |
ebi | rs476463 |
HLI | rs476463 |
Exac | rs476463 |
Gnomad | rs476463 |
Varsome | rs476463 |
LitVar | rs476463 |
Map | rs476463 |
PheGenI | rs476463 |
Biobank | rs476463 |
1000 genomes | rs476463 |
hgdp | rs476463 |
ensembl | rs476463 |
geneview | rs476463 |
scholar | rs476463 |
rs476463 | |
pharmgkb | rs476463 |
gwascentral | rs476463 |
openSNP | rs476463 |
23andMe | rs476463 |
SNPshot | rs476463 |
SNPdbe | rs476463 |
MSV3d | rs476463 |
GWAS Ctlg | rs476463 |
GMAF | 0.1653 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 20171287] |
Trait | Brain structure |
Title | Voxelwise Genome-Wide Association Study (vGWAS). |
Risk Allele | |
P-val | 0.000001 |
Odds Ratio | None None |