rs9257616
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs9257616(A;A) |
Make rs9257616(A;G) |
Make rs9257616(G;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 6 |
Position | 29212944 |
is a | snp |
is | mentioned by |
dbSNP | rs9257616 |
dbSNP (classic) | rs9257616 |
ClinGen | rs9257616 |
ebi | rs9257616 |
HLI | rs9257616 |
Exac | rs9257616 |
Gnomad | rs9257616 |
Varsome | rs9257616 |
LitVar | rs9257616 |
Map | rs9257616 |
PheGenI | rs9257616 |
Biobank | rs9257616 |
1000 genomes | rs9257616 |
hgdp | rs9257616 |
ensembl | rs9257616 |
geneview | rs9257616 |
scholar | rs9257616 |
rs9257616 | |
pharmgkb | rs9257616 |
gwascentral | rs9257616 |
openSNP | rs9257616 |
23andMe | rs9257616 |
SNPshot | rs9257616 |
SNPdbe | rs9257616 |
MSV3d | rs9257616 |
GWAS Ctlg | rs9257616 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 24047820] |
Trait | Social communication problems |
Title | Common variation contributes to the genetic architecture of social communication traits. |
Risk Allele | G |
P-val | 3E-7 |
Odds Ratio | .09 [0.058-0.128] unit increase |