rs4218
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs4218(C;C) |
Make rs4218(C;G) |
Make rs4218(G;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 15 |
Position | 59136459 |
Gene | MYO1E |
is a | snp |
is | mentioned by |
dbSNP | rs4218 |
dbSNP (classic) | rs4218 |
ClinGen | rs4218 |
ebi | rs4218 |
HLI | rs4218 |
Exac | rs4218 |
Gnomad | rs4218 |
Varsome | rs4218 |
LitVar | rs4218 |
Map | rs4218 |
PheGenI | rs4218 |
Biobank | rs4218 |
1000 genomes | rs4218 |
hgdp | rs4218 |
ensembl | rs4218 |
geneview | rs4218 |
scholar | rs4218 |
rs4218 | |
pharmgkb | rs4218 |
gwascentral | rs4218 |
openSNP | rs4218 |
23andMe | rs4218 |
SNPshot | rs4218 |
SNPdbe | rs4218 |
MSV3d | rs4218 |
GWAS Ctlg | rs4218 |
Max Magnitude | 0 |
? | (C;C) (C;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 | 1E-7 |
Odds Ratio | .10 [0.063-0.137] unit increase |