{{Rsnum
|rsid=122468182
|Chromosome=X
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=UPF3B
|position=119843293
|Gene_s=UPF3B
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=300298
|variant=0004
|rsnum=122468182
}}{{ClinVar
|rsid=122468182
|Reversed=1
|FwdREF=T
|FwdALT=G
|REF=A
|ALT=C
|RSPOS=118977256
|CHROM=X
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=UPF3B:65109
|GENE_NAME=UPF3B
|GENE_ID=65109
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.118977256A>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=300298.0004
|CLNSIG=5
|CLNCUI=C1970822
|CLNDBN=X-linked mental retardation, syndromic 14
|Disease=X-linked mental retardation
|CLNACC=RCV000012154.16
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1970822:300676:776
}}