{{Rsnum
|rsid=121434622
|Chromosome=X
|Orientation=plus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=FMR1
|position=147936534
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=FMR1
}}{{omim
|id=309550
|rsnum=121434622
|variant=0001
}}{{ClinVar
|rsid=121434622
|Reversed=0
|FwdREF=T
|FwdALT=A
|REF=T
|ALT=A
|RSPOS=147018053
|CHROM=X
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=FMR1:2332
|GENE_NAME=FMR1
|GENE_ID=2332
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.147018053T>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=309550.0001
|CLNSIG=5
|CLNCUI=C0016667
|CLNDBN=Fragile X syndrome
|Disease=Fragile X syndrome
|CLNACC=RCV000010648.1
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1384:C0016667:300624:908:613003
}}