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rs869312681

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs869312681(A;G)
Make rs869312681(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position9763169
GeneGRIN2A
is asnp
is mentioned by
dbSNPrs869312681
ebirs869312681
HLIrs869312681
Exacrs869312681
Varsomers869312681
Maprs869312681
PheGenIrs869312681
hapmaprs869312681
1000 genomesrs869312681
hgdprs869312681
ensemblrs869312681
gopubmedrs869312681
geneviewrs869312681
scholarrs869312681
googlers869312681
pharmgkbrs869312681
gwascentralrs869312681
openSNPrs869312681
23andMers869312681
23andMe allrs869312681
SNP Nexus

SNPshotrs869312681
SNPdbers869312681
MSV3drs869312681
GWAS Ctlgrs869312681
Max Magnitude0
ClinVar
Risk rs869312681(G;G)
Alt rs869312681(G;G)
Reference rs869312681(A;A)
Significance Probable-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.9857026T>C
CLNSRC
CLNACC RCV000209878.1,