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rs869312916

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs869312916(A;G)
Make rs869312916(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position9829589
GeneGRIN2A
is asnp
is mentioned by
dbSNPrs869312916
ebirs869312916
HLIrs869312916
Exacrs869312916
Varsomers869312916
Maprs869312916
PheGenIrs869312916
hapmaprs869312916
1000 genomesrs869312916
hgdprs869312916
ensemblrs869312916
gopubmedrs869312916
geneviewrs869312916
scholarrs869312916
googlers869312916
pharmgkbrs869312916
gwascentralrs869312916
openSNPrs869312916
23andMers869312916
23andMe allrs869312916
SNP Nexus

SNPshotrs869312916
SNPdbers869312916
MSV3drs869312916
GWAS Ctlgrs869312916
Max Magnitude0
ClinVar
Risk rs869312916(G;G)
Alt rs869312916(G;G)
Reference rs869312916(A;A)
Significance Pathogenic
Disease Inborn genetic diseases
Variation info
Gene GRIN2A
CLNDBN Inborn genetic diseases
Reversed 1
HGVS NC_000016.9:g.9923446T>C
CLNSRC
CLNACC RCV000210655.1,