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rs1085307961

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome16
Position9840703
GeneGRIN2A
is asnp
is mentioned by
dbSNPrs1085307961
dbSNP (old)rs1085307961
ClinGenrs1085307961
ebirs1085307961
HLIrs1085307961
Exacrs1085307961
Gnomadrs1085307961
Varsomers1085307961
Maprs1085307961
PheGenIrs1085307961
Biobankrs1085307961
1000 genomesrs1085307961
hgdprs1085307961
ensemblrs1085307961
gopubmedrs1085307961
geneviewrs1085307961
scholarrs1085307961
googlers1085307961
pharmgkbrs1085307961
gwascentralrs1085307961
openSNPrs1085307961
23andMers1085307961
23andMe allrs1085307961
SNPshotrs1085307961
SNPdbers1085307961
MSV3drs1085307961
GWAS Ctlgrs1085307961
Max Magnitude0
ClinVar
Risk rs1085307961(T;T)
Alt rs1085307961(T;T)
Reference Rs1085307961(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GRIN2A
CLNDBN not provided
Reversed 1
HGVS NC_000016.9:g.9934560C>A
CLNSRC
CLNACC RCV000489886.1,