{{Rsnum
|rsid=122459146
|Chromosome=X
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=FHL1
|position=136207909
|Gene_s=FHL1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=300163
|variant=0008
|rsnum=122459146
}}{{ClinVar
|rsid=122459146
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=135290068
|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.135290068G>A
|CLNORIGIN=1
|CLNSIG=5
|Tags=PM;OTHERKG;LSD;OM
|CLNACC=RCV000012310.21
|CLNDBN=MYOPATHY, REDUCING BODY, X-LINKED, SEVERE EARLY-ONSET
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=300163.0008
|Disease=MYOPATHY
}}