Have data from 23andMe or Ancestry? Make a report automatically with Promethease !

rs1057521810

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057521810(A;A)
Make rs1057521810(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position10180247
GeneGRIN2A
is asnp
is mentioned by
dbSNPrs1057521810
dbSNP (old)rs1057521810
ClinGenrs1057521810
ebirs1057521810
HLIrs1057521810
Exacrs1057521810
Gnomadrs1057521810
Varsomers1057521810
Maprs1057521810
PheGenIrs1057521810
Biobankrs1057521810
1000 genomesrs1057521810
hgdprs1057521810
ensemblrs1057521810
gopubmedrs1057521810
geneviewrs1057521810
scholarrs1057521810
googlers1057521810
pharmgkbrs1057521810
gwascentralrs1057521810
openSNPrs1057521810
23andMers1057521810
23andMe allrs1057521810
SNPshotrs1057521810
SNPdbers1057521810
MSV3drs1057521810
GWAS Ctlgrs1057521810
Max Magnitude0
ClinVar
Risk rs1057521810(A;A)
Alt rs1057521810(A;A)
Reference Rs1057521810(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GRIN2A
CLNDBN not provided
Reversed 1
HGVS NC_000016.9:g.10274104C>T
CLNSRC
CLNACC RCV000445092.1,