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rs797044849

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs797044849(C;C)
Make rs797044849(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position13567164
GeneGRIN2B
is asnp
is mentioned by
dbSNPrs797044849
ebirs797044849
HLIrs797044849
Exacrs797044849
Varsomers797044849
Maprs797044849
PheGenIrs797044849
hapmaprs797044849
1000 genomesrs797044849
hgdprs797044849
ensemblrs797044849
gopubmedrs797044849
geneviewrs797044849
scholarrs797044849
googlers797044849
pharmgkbrs797044849
gwascentralrs797044849
openSNPrs797044849
23andMers797044849
23andMe allrs797044849
SNP Nexus

SNPshotrs797044849
SNPdbers797044849
MSV3drs797044849
GWAS Ctlgrs797044849
Max Magnitude0
ClinVar
Risk rs797044849(C;C)
Alt rs797044849(C;C)
Reference rs797044849(G;G)
Significance Pathogenic
Disease not provided Inborn genetic diseases not specified
Variation info
Gene GRIN2B
CLNDBN not provided Inborn genetic diseases not specified
Reversed 1
HGVS NC_000012.11:g.13720098C>A; NC_000012.11:g.13720098C>G
CLNSRC
CLNACC RCV000217079.1, RCV000190648.1, RCV000235569.1,