{{Rsnum
|rsid=267606811
|Chromosome=X
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=FHL1
|position=136209392
|Gene_s=FHL1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=X
|CLNACC=RCV000012315.21
|CLNALLE=1
|CLNDBN=X-linked myopathy with postural muscle atrophy
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1436:C2678055:300696:261
|CLNHGVS=NC_000023.10:g.135291551G>A
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=300163.0013
|Disease=X-linked myopathy with postural muscle atrophy
|FwdALT=A
|FwdREF=G
|GENEINFO=FHL1:2273
|GENE_ID=2273
|GENE_NAME=FHL1
|REF=G
|RSPOS=135291551
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=267606811
}}