{{Rsnum
|rsid=122458141
|Chromosome=X
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=FHL1
|position=136208625
|Gene_s=FHL1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=300163
|variant=0002
|rsnum=122458141
}}{{ClinVar
|rsid=122458141
|Reversed=0
|FwdREF=C
|FwdALT=G
|REF=C
|ALT=G
|RSPOS=135290784
|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.135290784C>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=300163.0002
|CLNSIG=5
|CLNCUI=C2678055
|CLNDBN=X-linked myopathy with postural muscle atrophy
|Disease=X-linked myopathy with postural muscle atrophy
|CLNACC=RCV000012304.23
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1436:C2678055:300696:261
}}