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rs1064796752

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome12
Position13569848
GeneGRIN2B
is asnp
is mentioned by
dbSNPrs1064796752
dbSNP (old)rs1064796752
ClinGenrs1064796752
ebirs1064796752
HLIrs1064796752
Exacrs1064796752
Gnomadrs1064796752
Varsomers1064796752
Maprs1064796752
PheGenIrs1064796752
Biobankrs1064796752
1000 genomesrs1064796752
hgdprs1064796752
ensemblrs1064796752
gopubmedrs1064796752
geneviewrs1064796752
scholarrs1064796752
googlers1064796752
pharmgkbrs1064796752
gwascentralrs1064796752
openSNPrs1064796752
23andMers1064796752
23andMe allrs1064796752
SNPshotrs1064796752
SNPdbers1064796752
MSV3drs1064796752
GWAS Ctlgrs1064796752
Max Magnitude0
ClinVar
Risk rs1064796752(G;G)
Alt rs1064796752(G;G)
Reference Rs1064796752(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GRIN2B
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.13722782G>C
CLNSRC
CLNACC RCV000486259.1,