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rs1064796608

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome16
Position9768996
GeneGRIN2A
is asnp
is mentioned by
dbSNPrs1064796608
dbSNP (old)rs1064796608
ClinGenrs1064796608
ebirs1064796608
HLIrs1064796608
Exacrs1064796608
Gnomadrs1064796608
Varsomers1064796608
Maprs1064796608
PheGenIrs1064796608
Biobankrs1064796608
1000 genomesrs1064796608
hgdprs1064796608
ensemblrs1064796608
gopubmedrs1064796608
geneviewrs1064796608
scholarrs1064796608
googlers1064796608
pharmgkbrs1064796608
gwascentralrs1064796608
openSNPrs1064796608
23andMers1064796608
23andMe allrs1064796608
SNPshotrs1064796608
SNPdbers1064796608
MSV3drs1064796608
GWAS Ctlgrs1064796608
Max Magnitude0
ClinVar
Risk rs1064796608(G;G)
Alt rs1064796608(G;G)
Reference Rs1064796608(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene GRIN2A
CLNDBN not provided
Reversed 1
HGVS NC_000016.9:g.9862853A>C
CLNSRC
CLNACC RCV000479309.1,