rs7801303
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs7801303(A;A) |
Make rs7801303(A;G) |
Make rs7801303(G;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 7 |
Position | 40878471 |
Gene | LOC105375242 |
is a | snp |
is | mentioned by |
dbSNP | rs7801303 |
dbSNP (classic) | rs7801303 |
ClinGen | rs7801303 |
ebi | rs7801303 |
HLI | rs7801303 |
Exac | rs7801303 |
Gnomad | rs7801303 |
Varsome | rs7801303 |
LitVar | rs7801303 |
Map | rs7801303 |
PheGenI | rs7801303 |
Biobank | rs7801303 |
1000 genomes | rs7801303 |
hgdp | rs7801303 |
ensembl | rs7801303 |
geneview | rs7801303 |
scholar | rs7801303 |
rs7801303 | |
pharmgkb | rs7801303 |
gwascentral | rs7801303 |
openSNP | rs7801303 |
23andMe | rs7801303 |
SNPshot | rs7801303 |
SNPdbe | rs7801303 |
MSV3d | rs7801303 |
GWAS Ctlg | rs7801303 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 24571439] |
Trait | Parent of origin effect on language impairment (paternal) |
Title | Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairment. |
Risk Allele | |
P-val | 4E-7 |
Odds Ratio | NR NR |