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rs797045047

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs797045047(C;C)
Make rs797045047(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position137162510
GeneGRIN1
is asnp
is mentioned by
dbSNPrs797045047
ebirs797045047
HLIrs797045047
Exacrs797045047
Varsomers797045047
Maprs797045047
PheGenIrs797045047
hapmaprs797045047
1000 genomesrs797045047
hgdprs797045047
ensemblrs797045047
gopubmedrs797045047
geneviewrs797045047
scholarrs797045047
googlers797045047
pharmgkbrs797045047
gwascentralrs797045047
openSNPrs797045047
23andMers797045047
23andMe allrs797045047
SNP Nexus

SNPshotrs797045047
SNPdbers797045047
MSV3drs797045047
GWAS Ctlgrs797045047
Max Magnitude0
ClinVar
Risk rs797045047(C;C)
Alt rs797045047(C;C)
Reference rs797045047(G;G)
Significance Probable-Pathogenic
Disease Mental retardation
Variation info
Gene GRIN1
CLNDBN Mental retardation, autosomal dominant 8
Reversed 0
HGVS NC_000009.11:g.140056962G>C
CLNSRC Baylor College of Medicine
CLNACC RCV000191091.1,