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rs774592932

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs774592932(A;A)
Make rs774592932(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position13615213
GeneGRIN2B, LOC105369668
is asnp
is mentioned by
dbSNPrs774592932
dbSNP (classic)rs774592932
ClinGenrs774592932
ebirs774592932
HLIrs774592932
Exacrs774592932
Gnomadrs774592932
Varsomers774592932
LitVarrs774592932
Maprs774592932
PheGenIrs774592932
Biobankrs774592932
1000 genomesrs774592932
hgdprs774592932
ensemblrs774592932
geneviewrs774592932
scholarrs774592932
googlers774592932
pharmgkbrs774592932
gwascentralrs774592932
openSNPrs774592932
23andMers774592932
23andMe allrs774592932
SNPshotrs774592932
SNPdbers774592932
MSV3drs774592932
GWAS Ctlgrs774592932
Max Magnitude0
ClinVar
Risk rs774592932(A;A)
Alt rs774592932(A;A)
Reference Rs774592932(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene GRIN2B
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.13768147G>A
CLNSRC
CLNACC RCV000426345.1,