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rs864309560

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs864309560(A;A)
Make rs864309560(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position13567193
GeneGRIN2B
is asnp
is mentioned by
dbSNPrs864309560
ebirs864309560
HLIrs864309560
Exacrs864309560
Varsomers864309560
Maprs864309560
PheGenIrs864309560
hapmaprs864309560
1000 genomesrs864309560
hgdprs864309560
ensemblrs864309560
gopubmedrs864309560
geneviewrs864309560
scholarrs864309560
googlers864309560
pharmgkbrs864309560
gwascentralrs864309560
openSNPrs864309560
23andMers864309560
23andMe allrs864309560
SNP Nexus

SNPshotrs864309560
SNPdbers864309560
MSV3drs864309560
GWAS Ctlgrs864309560
Max Magnitude0
ClinVar
Risk rs864309560(A;A)
Alt rs864309560(A;A)
Reference rs864309560(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene GRIN2B
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.13720127G>T
CLNSRC
CLNACC RCV000203067.1,