rs11819364
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs11819364(A;A) |
Make rs11819364(A;C) |
Make rs11819364(C;C) |
Reference | GRCh38 38.1/142 |
Chromosome | 10 |
Position | 127245046 |
Gene | DOCK1 |
is a | snp |
is | mentioned by |
dbSNP | rs11819364 |
dbSNP (classic) | rs11819364 |
ClinGen | rs11819364 |
ebi | rs11819364 |
HLI | rs11819364 |
Exac | rs11819364 |
Gnomad | rs11819364 |
Varsome | rs11819364 |
LitVar | rs11819364 |
Map | rs11819364 |
PheGenI | rs11819364 |
Biobank | rs11819364 |
1000 genomes | rs11819364 |
hgdp | rs11819364 |
ensembl | rs11819364 |
geneview | rs11819364 |
scholar | rs11819364 |
rs11819364 | |
pharmgkb | rs11819364 |
gwascentral | rs11819364 |
openSNP | rs11819364 |
23andMe | rs11819364 |
SNPshot | rs11819364 |
SNPdbe | rs11819364 |
MSV3d | rs11819364 |
GWAS Ctlg | rs11819364 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 24564958] |
Trait | Social communication problems |
Title | Variability in the common genetic architecture of social-communication spectrum phenotypes during childhood and adolescence. |
Risk Allele | C |
P-val | 9E-6 |
Odds Ratio | .32 [0.18-0.46] unit increase |