{{Rsnum
|rsid=137852352
|Chromosome=X
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=GRIA3
|position=123464905
|Gene_s=GRIA3
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=305915
|variant=0003
|rsnum=137852352
}}{{ClinVar
|rsid=137852352
|Reversed=0
|FwdREF=T
|FwdALT=C
|REF=T
|ALT=C
|RSPOS=122598756
|CHROM=X
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=GRIA3:2892
|GENE_NAME=GRIA3
|GENE_ID=2892
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.122598756T>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=305915.0003
|CLNSIG=5
|CLNCUI=C2678051
|CLNDBN=Mental retardation, X-linked, syndromic, wu type
|Disease=Mental retardation
|CLNACC=RCV000011071.4
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C2678051:300699
}}