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rs878853143

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs878853143(C;G)
Make rs878853143(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome9
Position137162209
GeneGRIN1
is asnp
is mentioned by
dbSNPrs878853143
ebirs878853143
HLIrs878853143
Exacrs878853143
Varsomers878853143
Maprs878853143
PheGenIrs878853143
hapmaprs878853143
1000 genomesrs878853143
hgdprs878853143
ensemblrs878853143
gopubmedrs878853143
geneviewrs878853143
scholarrs878853143
googlers878853143
pharmgkbrs878853143
gwascentralrs878853143
openSNPrs878853143
23andMers878853143
23andMe allrs878853143
SNP Nexus

SNPshotrs878853143
SNPdbers878853143
MSV3drs878853143
GWAS Ctlgrs878853143
Max Magnitude0
ClinVar
Risk rs878853143(G;G)
Alt rs878853143(G;G)
Reference rs878853143(C;C)
Significance Pathogenic
Disease Intellectual disability
Variation info
Gene GRIN1
CLNDBN Intellectual disability
Reversed 0
HGVS NC_000009.11:g.140056661C>G
CLNSRC
CLNACC RCV000224047.1,