rs2253478
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs2253478(A;A) |
Make rs2253478(A;G) |
Make rs2253478(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 7 |
Position | 114337941 |
Gene | FOXP2 |
is a | snp |
is | mentioned by |
dbSNP | rs2253478 |
dbSNP (classic) | rs2253478 |
ClinGen | rs2253478 |
ebi | rs2253478 |
HLI | rs2253478 |
Exac | rs2253478 |
Gnomad | rs2253478 |
Varsome | rs2253478 |
LitVar | rs2253478 |
Map | rs2253478 |
PheGenI | rs2253478 |
Biobank | rs2253478 |
1000 genomes | rs2253478 |
hgdp | rs2253478 |
ensembl | rs2253478 |
geneview | rs2253478 |
scholar | rs2253478 |
rs2253478 | |
pharmgkb | rs2253478 |
gwascentral | rs2253478 |
openSNP | rs2253478 |
23andMe | rs2253478 |
SNPshot | rs2253478 |
SNPdbe | rs2253478 |
MSV3d | rs2253478 |
GWAS Ctlg | rs2253478 |
GMAF | 0.3549 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 20649982] FOXP2 gene and language impairment in schizophrenia: association and epigenetic studies