rs9390754
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs9390754(A;A) |
Make rs9390754(A;G) |
Make rs9390754(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 6 |
Position | 101517038 |
Gene | GRIK2 |
is a | snp |
is | mentioned by |
dbSNP | rs9390754 |
dbSNP (classic) | rs9390754 |
ClinGen | rs9390754 |
ebi | rs9390754 |
HLI | rs9390754 |
Exac | rs9390754 |
Gnomad | rs9390754 |
Varsome | rs9390754 |
LitVar | rs9390754 |
Map | rs9390754 |
PheGenI | rs9390754 |
Biobank | rs9390754 |
1000 genomes | rs9390754 |
hgdp | rs9390754 |
ensembl | rs9390754 |
geneview | rs9390754 |
scholar | rs9390754 |
rs9390754 | |
pharmgkb | rs9390754 |
gwascentral | rs9390754 |
openSNP | rs9390754 |
23andMe | rs9390754 |
SNPshot | rs9390754 |
SNPdbe | rs9390754 |
MSV3d | rs9390754 |
GWAS Ctlg | rs9390754 |
GMAF | 0.2663 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
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[PMID 22116939] Two-stage genome-wide association study identifies variants in CAMSAP1L1 as susceptibility loci for epilepsy in Chinese
[PMID 27324535] [Association between glutamate receptor 2 polymorphisms and epilepsy in children].