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rs1064794979

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome12
Position13567146
GeneGRIN2B
is asnp
is mentioned by
dbSNPrs1064794979
dbSNP (old)rs1064794979
ClinGenrs1064794979
ebirs1064794979
HLIrs1064794979
Exacrs1064794979
Gnomadrs1064794979
Varsomers1064794979
LitVarrs1064794979
Maprs1064794979
PheGenIrs1064794979
Biobankrs1064794979
1000 genomesrs1064794979
hgdprs1064794979
ensemblrs1064794979
gopubmedrs1064794979
geneviewrs1064794979
scholarrs1064794979
googlers1064794979
pharmgkbrs1064794979
gwascentralrs1064794979
openSNPrs1064794979
23andMers1064794979
23andMe allrs1064794979
SNPshotrs1064794979
SNPdbers1064794979
MSV3drs1064794979
GWAS Ctlgrs1064794979
Max Magnitude0
ClinVar
Risk rs1064794979(A;A)
Alt rs1064794979(A;A)
Reference Rs1064794979(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GRIN2B
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.13720080C>T
CLNSRC
CLNACC RCV000480326.1,