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

rs876661102

From SNPedia

Orientationminus
Geno Mag Summary
(AAG;AAG) 0 common in clinvar
Make rs876661102(-;-)
Make rs876661102(-;AAG)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position13564310
GeneGRIN2B
is asnp
is mentioned by
dbSNPrs876661102
ebirs876661102
HLIrs876661102
Exacrs876661102
Varsomers876661102
Maprs876661102
PheGenIrs876661102
hapmaprs876661102
1000 genomesrs876661102
hgdprs876661102
ensemblrs876661102
gopubmedrs876661102
geneviewrs876661102
scholarrs876661102
googlers876661102
pharmgkbrs876661102
gwascentralrs876661102
openSNPrs876661102
23andMers876661102
23andMe allrs876661102
SNP Nexus

SNPshotrs876661102
SNPdbers876661102
MSV3drs876661102
GWAS Ctlgrs876661102
Max Magnitude0
ClinVar
Risk rs876661102(;)
Alt rs876661102(;)
Reference rs876661102(AAG;AAG)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GRIN2B
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.13717244_13717246delCTT
CLNSRC
CLNACC RCV000223164.1,