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rs1064796658

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome16
Position9764370
GeneGRIN2A
is asnp
is mentioned by
dbSNPrs1064796658
dbSNP (old)rs1064796658
ClinGenrs1064796658
ebirs1064796658
HLIrs1064796658
Exacrs1064796658
Gnomadrs1064796658
Varsomers1064796658
Maprs1064796658
PheGenIrs1064796658
Biobankrs1064796658
1000 genomesrs1064796658
hgdprs1064796658
ensemblrs1064796658
gopubmedrs1064796658
geneviewrs1064796658
scholarrs1064796658
googlers1064796658
pharmgkbrs1064796658
gwascentralrs1064796658
openSNPrs1064796658
23andMers1064796658
23andMe allrs1064796658
SNPshotrs1064796658
SNPdbers1064796658
MSV3drs1064796658
GWAS Ctlgrs1064796658
Max Magnitude0
ClinVar
Risk rs1064796658(A;A)
Alt rs1064796658(A;A)
Reference Rs1064796658(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GRIN2A
CLNDBN not provided
Reversed 1
HGVS NC_000016.9:g.9858227G>T
CLNSRC
CLNACC RCV000484465.1,