rs12342373
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs12342373(A;A) |
Make rs12342373(A;G) |
Make rs12342373(G;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 9 |
Position | 126640288 |
Gene | LMX1B |
is a | snp |
is | mentioned by |
dbSNP | rs12342373 |
dbSNP (classic) | rs12342373 |
ClinGen | rs12342373 |
ebi | rs12342373 |
HLI | rs12342373 |
Exac | rs12342373 |
Gnomad | rs12342373 |
Varsome | rs12342373 |
LitVar | rs12342373 |
Map | rs12342373 |
PheGenI | rs12342373 |
Biobank | rs12342373 |
1000 genomes | rs12342373 |
hgdp | rs12342373 |
ensembl | rs12342373 |
geneview | rs12342373 |
scholar | rs12342373 |
rs12342373 | |
pharmgkb | rs12342373 |
gwascentral | rs12342373 |
openSNP | rs12342373 |
23andMe | rs12342373 |
SNPshot | rs12342373 |
SNPdbe | rs12342373 |
MSV3d | rs12342373 |
GWAS Ctlg | rs12342373 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 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 | A |
P-val | 3E-6 |
Odds Ratio | .19 [0.11-0.27] unit increase |