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rs387906635

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387906635(A;A)
Make rs387906635(A;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position137162710
GeneGRIN1
is asnp
is mentioned by
dbSNPrs387906635
dbSNP (old)rs387906635
ClinGenrs387906635
ebirs387906635
HLIrs387906635
Exacrs387906635
Varsomers387906635
Maprs387906635
PheGenIrs387906635
Biobankrs387906635
1000 genomesrs387906635
hgdprs387906635
ensemblrs387906635
gopubmedrs387906635
geneviewrs387906635
scholarrs387906635
googlers387906635
pharmgkbrs387906635
gwascentralrs387906635
openSNPrs387906635
23andMers387906635
23andMe allrs387906635
SNP Nexus

SNPshotrs387906635
SNPdbers387906635
MSV3drs387906635
GWAS Ctlgrs387906635
Max Magnitude0
ClinVar
Risk rs387906635(A;A)
Alt rs387906635(A;A)
Reference Rs387906635(G;G)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene GRIN1
CLNDBN Mental retardation, autosomal dominant 8
Reversed 0
HGVS NC_000009.11:g.140057162G>A
CLNSRC OMIM Allelic Variant UniProtKB (protein)
CLNACC RCV000022577.27,