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rs1085307547

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome12
Position13567108
GeneGRIN2B
is asnp
is mentioned by
dbSNPrs1085307547
dbSNP (old)rs1085307547
ClinGenrs1085307547
ebirs1085307547
HLIrs1085307547
Exacrs1085307547
Gnomadrs1085307547
Varsomers1085307547
LitVarrs1085307547
Maprs1085307547
PheGenIrs1085307547
Biobankrs1085307547
1000 genomesrs1085307547
hgdprs1085307547
ensemblrs1085307547
gopubmedrs1085307547
geneviewrs1085307547
scholarrs1085307547
googlers1085307547
pharmgkbrs1085307547
gwascentralrs1085307547
openSNPrs1085307547
23andMers1085307547
23andMe allrs1085307547
SNPshotrs1085307547
SNPdbers1085307547
MSV3drs1085307547
GWAS Ctlgrs1085307547
Max Magnitude0
ClinVar
Risk rs1085307547(A;A)
Alt rs1085307547(A;A)
Reference Rs1085307547(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GRIN2B
CLNDBN not provided
Reversed 1
HGVS NC_000012.11:g.13720042C>T
CLNSRC
CLNACC RCV000488929.1,