rs296859
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs296859(A;A) |
Make rs296859(A;G) |
Make rs296859(G;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 9 |
Position | 4774015 |
is a | snp |
is | mentioned by |
dbSNP | rs296859 |
dbSNP (classic) | rs296859 |
ClinGen | rs296859 |
ebi | rs296859 |
HLI | rs296859 |
Exac | rs296859 |
Gnomad | rs296859 |
Varsome | rs296859 |
LitVar | rs296859 |
Map | rs296859 |
PheGenI | rs296859 |
Biobank | rs296859 |
1000 genomes | rs296859 |
hgdp | rs296859 |
ensembl | rs296859 |
geneview | rs296859 |
scholar | rs296859 |
rs296859 | |
pharmgkb | rs296859 |
gwascentral | rs296859 |
openSNP | rs296859 |
23andMe | rs296859 |
SNPshot | rs296859 |
SNPdbe | rs296859 |
MSV3d | rs296859 |
GWAS Ctlg | rs296859 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 24065183] |
Trait | Handedness |
Title | Genome-wide association study of handedness excludes simple genetic models. |
Risk Allele | |
P-val | 4E-7 |
Odds Ratio | NR NR |