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rs1057518070

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057518070(G;G)
Make rs1057518070(G;T)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position9822294
GeneGRIN2A
is asnp
is mentioned by
dbSNPrs1057518070
dbSNP (old)rs1057518070
ClinGenrs1057518070
ebirs1057518070
HLIrs1057518070
Exacrs1057518070
Gnomadrs1057518070
Varsomers1057518070
Maprs1057518070
PheGenIrs1057518070
Biobankrs1057518070
1000 genomesrs1057518070
hgdprs1057518070
ensemblrs1057518070
gopubmedrs1057518070
geneviewrs1057518070
scholarrs1057518070
googlers1057518070
pharmgkbrs1057518070
gwascentralrs1057518070
openSNPrs1057518070
23andMers1057518070
23andMe allrs1057518070
SNPshotrs1057518070
SNPdbers1057518070
MSV3drs1057518070
GWAS Ctlgrs1057518070
Max Magnitude0
ClinVar
Risk rs1057518070(G;G)
Alt rs1057518070(G;G)
Reference Rs1057518070(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GRIN2A
CLNDBN not provided
Reversed 1
HGVS NC_000016.9:g.9916151A>C
CLNSRC
CLNACC RCV000413937.1,