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rs1057521729

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057521729(A;A)
Make rs1057521729(A;G)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position123465757
GeneGRIA3
is asnp
is mentioned by
dbSNPrs1057521729
dbSNP (old)rs1057521729
ClinGenrs1057521729
ebirs1057521729
HLIrs1057521729
Exacrs1057521729
Gnomadrs1057521729
Varsomers1057521729
Maprs1057521729
PheGenIrs1057521729
Biobankrs1057521729
1000 genomesrs1057521729
hgdprs1057521729
ensemblrs1057521729
gopubmedrs1057521729
geneviewrs1057521729
scholarrs1057521729
googlers1057521729
pharmgkbrs1057521729
gwascentralrs1057521729
openSNPrs1057521729
23andMers1057521729
23andMe allrs1057521729
SNPshotrs1057521729
SNPdbers1057521729
MSV3drs1057521729
GWAS Ctlgrs1057521729
Max Magnitude0
ClinVar
Risk rs1057521729(A;A)
Alt rs1057521729(A;A)
Reference Rs1057521729(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GRIA3
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.122599608G>A
CLNSRC
CLNACC RCV000427181.1,