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rs587777361

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587777361(C;C)
Make rs587777361(C;G)
ReferenceGRCh38 38.1/142
ChromosomeX
Position123427951
GeneGRIA3
is asnp
is mentioned by
dbSNPrs587777361
ebirs587777361
HLIrs587777361
Exacrs587777361
Varsomers587777361
Maprs587777361
PheGenIrs587777361
hapmaprs587777361
1000 genomesrs587777361
hgdprs587777361
ensemblrs587777361
gopubmedrs587777361
geneviewrs587777361
scholarrs587777361
googlers587777361
pharmgkbrs587777361
gwascentralrs587777361
openSNPrs587777361
23andMers587777361
23andMe allrs587777361
SNP Nexus

SNPshotrs587777361
SNPdbers587777361
MSV3drs587777361
GWAS Ctlgrs587777361
Max Magnitude0
ClinVar
Risk rs587777361(C;C)
Alt rs587777361(C;C)
Reference rs587777361(G;G)
Significance Pathogenic
Disease Mental retardation
Variation info
Gene GRIA3
CLNDBN Mental retardation, X-linked, syndromic, wu type
Reversed 0
HGVS NC_000023.10:g.122561802G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000115024.2,