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rs9390754

From SNPedia

Orientationplus
Stabilizedplus
Make rs9390754(A;A)
Make rs9390754(A;G)
Make rs9390754(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position101517038
GeneGRIK2
is asnp
is mentioned by
dbSNPrs9390754
ebirs9390754
HLIrs9390754
Exacrs9390754
Varsomers9390754
Maprs9390754
PheGenIrs9390754
hapmaprs9390754
1000 genomesrs9390754
hgdprs9390754
ensemblrs9390754
gopubmedrs9390754
geneviewrs9390754
scholarrs9390754
googlers9390754
pharmgkbrs9390754
gwascentralrs9390754
openSNPrs9390754
23andMers9390754
23andMe allrs9390754
SNP Nexus

SNPshotrs9390754
SNPdbers9390754
MSV3drs9390754
GWAS Ctlgrs9390754
GMAF0.2663
Max Magnitude
? (A;A) (A;G) (G;G) 28

[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].