Have questions? Visit https://www.reddit.com/r/SNPedia

rs876661167

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876661167(A;A)
Make rs876661167(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position13563906
GeneGRIN2B
is asnp
is mentioned by
dbSNPrs876661167
ebirs876661167
HLIrs876661167
Exacrs876661167
Varsomers876661167
Maprs876661167
PheGenIrs876661167
hapmaprs876661167
1000 genomesrs876661167
hgdprs876661167
ensemblrs876661167
gopubmedrs876661167
geneviewrs876661167
scholarrs876661167
googlers876661167
pharmgkbrs876661167
gwascentralrs876661167
openSNPrs876661167
23andMers876661167
23andMe allrs876661167
SNP Nexus

SNPshotrs876661167
SNPdbers876661167
MSV3drs876661167
GWAS Ctlgrs876661167
Max Magnitude0
ClinVar
Risk rs876661167(A;A)
Alt rs876661167(A;A)
Reference rs876661167(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GRIN2B
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.13716840C>T
CLNSRC
CLNACC RCV000214952.1,