rs17098356
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs17098356(G;G) |
Make rs17098356(G;T) |
Make rs17098356(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 14 |
Position | 61432121 |
Gene | PRKCH |
is a | snp |
is | mentioned by |
dbSNP | rs17098356 |
dbSNP (classic) | rs17098356 |
ClinGen | rs17098356 |
ebi | rs17098356 |
HLI | rs17098356 |
Exac | rs17098356 |
Gnomad | rs17098356 |
Varsome | rs17098356 |
LitVar | rs17098356 |
Map | rs17098356 |
PheGenI | rs17098356 |
Biobank | rs17098356 |
1000 genomes | rs17098356 |
hgdp | rs17098356 |
ensembl | rs17098356 |
geneview | rs17098356 |
scholar | rs17098356 |
rs17098356 | |
pharmgkb | rs17098356 |
gwascentral | rs17098356 |
openSNP | rs17098356 |
23andMe | rs17098356 |
SNPshot | rs17098356 |
SNPdbe | rs17098356 |
MSV3d | rs17098356 |
GWAS Ctlg | rs17098356 |
GMAF | 0.3214 |
Max Magnitude | 0 |
? | (G;G) (G;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 23738518] |
Trait | Reading and spelling |
Title | A genome-wide association study for reading and language abilities in two population cohorts. |
Risk Allele | |
P-val | 6E-6 |
Odds Ratio | NR NR |