{{Rsnum
|rsid=122458140
|Chromosome=X
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=FHL1
|position=136207825
|Gene_s=FHL1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=300163
|variant=0001
|rsnum=122458140
}}{{ClinVar
|rsid=122458140
|Reversed=0
|FwdREF=G
|FwdALT=C
|REF=G
|ALT=C
|RSPOS=135289984
|CHROM=X
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=FHL1:2273
|GENE_NAME=FHL1
|GENE_ID=2273
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.135289984G>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=300163.0001
|CLNSIG=5
|CLNCUI=C2678061
|CLNDBN=X-linked dominant scapuloperoneal myopathy
|Disease=X-linked dominant scapuloperoneal myopathy
|CLNACC=RCV000012303.23
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C2678061:300695
}}