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rs144902457

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs144902457(C;C)
Make rs144902457(C;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position123253500
GeneGRIA3
is asnp
is mentioned by
dbSNPrs144902457
ebirs144902457
HLIrs144902457
Exacrs144902457
Varsomers144902457
Maprs144902457
PheGenIrs144902457
hapmaprs144902457
1000 genomesrs144902457
hgdprs144902457
ensemblrs144902457
gopubmedrs144902457
geneviewrs144902457
scholarrs144902457
googlers144902457
pharmgkbrs144902457
gwascentralrs144902457
openSNPrs144902457
23andMers144902457
23andMe allrs144902457
SNP Nexus

SNPshotrs144902457
SNPdbers144902457
MSV3drs144902457
GWAS Ctlgrs144902457
Max Magnitude0
ClinVar
Risk rs144902457(C;C)
Alt rs144902457(C;C)
Reference rs144902457(T;T)
Significance Probable-Pathogenic
Disease Mental retardation
Variation info
Gene GRIA3
CLNDBN Mental retardation, X-linked, syndromic, wu type
Reversed 0
HGVS NC_000023.10:g.122387351T>C
CLNSRC
CLNACC RCV000209928.1,