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rs876661041

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs876661041(A;G)
Make rs876661041(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position13608643
GeneGRIN2B, LOC105369668
is asnp
is mentioned by
dbSNPrs876661041
ebirs876661041
HLIrs876661041
Exacrs876661041
Varsomers876661041
Maprs876661041
PheGenIrs876661041
hapmaprs876661041
1000 genomesrs876661041
hgdprs876661041
ensemblrs876661041
gopubmedrs876661041
geneviewrs876661041
scholarrs876661041
googlers876661041
pharmgkbrs876661041
gwascentralrs876661041
openSNPrs876661041
23andMers876661041
23andMe allrs876661041
SNP Nexus

SNPshotrs876661041
SNPdbers876661041
MSV3drs876661041
GWAS Ctlgrs876661041
Max Magnitude0
ClinVar
Risk rs876661041(G;G)
Alt rs876661041(G;G)
Reference rs876661041(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GRIN2B
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.13761577T>C
CLNSRC
CLNACC RCV000215266.1,