{{Rsnum
|rsid=122458145
|Chromosome=X
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=FHL1
|position=136207918
|Gene_s=FHL1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=300163
|variant=0007
|rsnum=122458145
}}{{ClinVar
|rsid=122458145
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=135290077
|CHROM=X
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=FHL1:2273
|GENE_NAME=FHL1
|GENE_ID=2273
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.135290077G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=300163.0007
|CLNSIG=5
|CLNCUI=C2678015
|CLNDBN=Myopathy, reducing body, X-linked, childhood-onset
|Disease=Myopathy
|CLNACC=RCV000012309.13
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C2678015:300718:97239
}}