{{Rsnum
|rsid=137854523
|Gene=ANO5
|Chromosome=11
|position=22236206
|Orientation=plus
|GMAF=0.0004591
|Gene_s=ANO5
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
}}{{omim
|id=608662
|variant=0005
|rsnum=137854523
}}{{ClinVar
|rsid=137854523
|Reversed=0
|FwdREF=G
|FwdALT=T
|REF=G
|ALT=T
|RSPOS=22257752
|CHROM=11
|GMAF=0.0005
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050168000000040016110100
|GENEINFO=ANO5:203859
|GENE_NAME=ANO5
|GENE_ID=203859
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.22257752G>T
|CLNSRC=Emory University; GeneReviews; OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=8801; NBK114459; 608662.0005
|CLNSIG=5
|CLNCUI=C1969785
|CLNDBN=Limb-girdle muscular dystrophy, type 2L; not provided
|Disease=Limb-girdle muscular dystrophy; not provided
|CLNACC=RCV000002249.1; RCV000082853.1
|Tags=PM;PMC;SLO;VLD;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9995; 0.0004591
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK114459:C1969785:611307:206549
|COMMON=0
}}{{PMID|20096397|OA=1
}} Recessive mutations in the putative calcium-activated chloride channel Anoctamin 5 cause proximal LGMD2L and distal MMD3 muscular dystrophies.