{{Rsnum
|rsid=122458142
|Chromosome=X
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=FHL1
|position=136207827
|Gene_s=FHL1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=300163
|variant=0004
|rsnum=122458142
}}{{ClinVar
|rsid=122458142
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=135289986
|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.135289986C>T
|CLNORIGIN=1
|CLNSIG=5
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNACC=RCV000012306.21
|CLNDBN=MYOPATHY, REDUCING BODY, X-LINKED, SEVERE EARLY-ONSET
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=300163.0004
|Disease=MYOPATHY
}}