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rs1057524089

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057524089(C;T)
Make rs1057524089(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position9938479
GeneGRIN2A
is asnp
is mentioned by
dbSNPrs1057524089
dbSNP (old)rs1057524089
ClinGenrs1057524089
ebirs1057524089
HLIrs1057524089
Exacrs1057524089
Gnomadrs1057524089
Varsomers1057524089
Maprs1057524089
PheGenIrs1057524089
Biobankrs1057524089
1000 genomesrs1057524089
hgdprs1057524089
ensemblrs1057524089
gopubmedrs1057524089
geneviewrs1057524089
scholarrs1057524089
googlers1057524089
pharmgkbrs1057524089
gwascentralrs1057524089
openSNPrs1057524089
23andMers1057524089
23andMe allrs1057524089
SNPshotrs1057524089
SNPdbers1057524089
MSV3drs1057524089
GWAS Ctlgrs1057524089
Max Magnitude0
ClinVar
Risk rs1057524089(T;T)
Alt rs1057524089(T;T)
Reference Rs1057524089(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene GRIN2A
CLNDBN not provided
Reversed 1
HGVS NC_000016.9:g.10032336G>A
CLNSRC
CLNACC RCV000438586.1,