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rs869312865

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869312865(C;C)
Make rs869312865(C;G)
ReferenceGRCh38.p2 38.2/147
Chromosome9
Position137156676
GeneGRIN1, LOC105376328
is asnp
is mentioned by
dbSNPrs869312865
ebirs869312865
HLIrs869312865
Exacrs869312865
Varsomers869312865
Maprs869312865
PheGenIrs869312865
hapmaprs869312865
1000 genomesrs869312865
hgdprs869312865
ensemblrs869312865
gopubmedrs869312865
geneviewrs869312865
scholarrs869312865
googlers869312865
pharmgkbrs869312865
gwascentralrs869312865
openSNPrs869312865
23andMers869312865
23andMe allrs869312865
SNP Nexus

SNPshotrs869312865
SNPdbers869312865
MSV3drs869312865
GWAS Ctlgrs869312865
Max Magnitude0
ClinVar
Risk rs869312865(C;C)
Alt rs869312865(C;C)
Reference rs869312865(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.140051128G>C
CLNSRC
CLNACC RCV000210389.1,