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rs387906637

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs387906637(C;T)
Make rs387906637(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position9938314
GeneGRIN2A
is asnp
is mentioned by
dbSNPrs387906637
ebirs387906637
HLIrs387906637
Exacrs387906637
Varsomers387906637
Maprs387906637
PheGenIrs387906637
hapmaprs387906637
1000 genomesrs387906637
hgdprs387906637
ensemblrs387906637
gopubmedrs387906637
geneviewrs387906637
scholarrs387906637
googlers387906637
pharmgkbrs387906637
gwascentralrs387906637
openSNPrs387906637
23andMers387906637
23andMe allrs387906637
SNP Nexus

SNPshotrs387906637
SNPdbers387906637
MSV3drs387906637
GWAS Ctlgrs387906637
Max Magnitude0
ClinVar
Risk rs387906637(T;T)
Alt rs387906637(T;T)
Reference rs387906637(C;C)
Significance Pathogenic
Disease Epilepsy
Variation info
Gene GRIN2A
CLNDBN Epilepsy, focal, with speech disorder and with or without mental retardation
Reversed 1
HGVS NC_000016.9:g.10032171G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000022584.24,