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rs1057521721

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057521721(A;A)
Make rs1057521721(A;G)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position123428020
GeneGRIA3
is asnp
is mentioned by
dbSNPrs1057521721
dbSNP (old)rs1057521721
ClinGenrs1057521721
ebirs1057521721
HLIrs1057521721
Exacrs1057521721
Gnomadrs1057521721
Varsomers1057521721
LitVarrs1057521721
Maprs1057521721
PheGenIrs1057521721
Biobankrs1057521721
1000 genomesrs1057521721
hgdprs1057521721
ensemblrs1057521721
gopubmedrs1057521721
geneviewrs1057521721
scholarrs1057521721
googlers1057521721
pharmgkbrs1057521721
gwascentralrs1057521721
openSNPrs1057521721
23andMers1057521721
23andMe allrs1057521721
SNPshotrs1057521721
SNPdbers1057521721
MSV3drs1057521721
GWAS Ctlgrs1057521721
Max Magnitude0
ClinVar
Risk rs1057521721(A;A)
Alt rs1057521721(A;A)
Reference Rs1057521721(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GRIA3
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.122561871G>A
CLNSRC
CLNACC RCV000426311.1,