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rs1057520116

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057520116(C;T)
Make rs1057520116(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position9829535
GeneGRIN2A
is asnp
is mentioned by
dbSNPrs1057520116
dbSNP (old)rs1057520116
ClinGenrs1057520116
ebirs1057520116
HLIrs1057520116
Exacrs1057520116
Gnomadrs1057520116
Varsomers1057520116
Maprs1057520116
PheGenIrs1057520116
Biobankrs1057520116
1000 genomesrs1057520116
hgdprs1057520116
ensemblrs1057520116
gopubmedrs1057520116
geneviewrs1057520116
scholarrs1057520116
googlers1057520116
pharmgkbrs1057520116
gwascentralrs1057520116
openSNPrs1057520116
23andMers1057520116
23andMe allrs1057520116
SNPshotrs1057520116
SNPdbers1057520116
MSV3drs1057520116
GWAS Ctlgrs1057520116
Max Magnitude0
ClinVar
Risk rs1057520116(T;T)
Alt rs1057520116(T;T)
Reference Rs1057520116(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GRIN2A
CLNDBN not provided
Reversed 1
HGVS NC_000016.9:g.9923392G>A
CLNSRC
CLNACC RCV000441603.1,