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rs1057523843

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057523843(C;C)
Make rs1057523843(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position9840656
GeneGRIN2A
is asnp
is mentioned by
dbSNPrs1057523843
dbSNP (classic)rs1057523843
ClinGenrs1057523843
ebirs1057523843
HLIrs1057523843
Exacrs1057523843
Gnomadrs1057523843
Varsomers1057523843
LitVarrs1057523843
Maprs1057523843
PheGenIrs1057523843
Biobankrs1057523843
1000 genomesrs1057523843
hgdprs1057523843
ensemblrs1057523843
geneviewrs1057523843
scholarrs1057523843
googlers1057523843
pharmgkbrs1057523843
gwascentralrs1057523843
openSNPrs1057523843
23andMers1057523843
23andMe allrs1057523843
SNPshotrs1057523843
SNPdbers1057523843
MSV3drs1057523843
GWAS Ctlgrs1057523843
Max Magnitude0
ClinVar
Risk rs1057523843(C;C)
Alt rs1057523843(C;C)
Reference Rs1057523843(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GRIN2A
CLNDBN not provided
Reversed 1
HGVS NC_000016.9:g.9934513C>G
CLNSRC
CLNACC RCV000441942.1,