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rs1064794679

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome16
Position9768846
GeneGRIN2A
is asnp
is mentioned by
dbSNPrs1064794679
dbSNP (classic)rs1064794679
ClinGenrs1064794679
ebirs1064794679
HLIrs1064794679
Exacrs1064794679
Gnomadrs1064794679
Varsomers1064794679
LitVarrs1064794679
Maprs1064794679
PheGenIrs1064794679
Biobankrs1064794679
1000 genomesrs1064794679
hgdprs1064794679
ensemblrs1064794679
geneviewrs1064794679
scholarrs1064794679
googlers1064794679
pharmgkbrs1064794679
gwascentralrs1064794679
openSNPrs1064794679
23andMers1064794679
23andMe allrs1064794679
SNPshotrs1064794679
SNPdbers1064794679
MSV3drs1064794679
GWAS Ctlgrs1064794679
Max Magnitude0
ClinVar
Risk rs1064794679(C;C)
Alt rs1064794679(C;C)
Reference Rs1064794679(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GRIN2A
CLNDBN not provided
Reversed 1
HGVS NC_000016.9:g.9862703C>G
CLNSRC
CLNACC RCV000479259.1,