{{Rsnum
|rsid=137854524
|Chromosome=11
|position=22255485
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=ANO5
|Gene_s=ANO5
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=608662
|variant=0003
|rsnum=137854524
}}{{ClinVar
|rsid=137854524
|Reversed=0
|FwdREF=C
|FwdALT=G
|REF=C
|ALT=G
|RSPOS=22277031
|CHROM=11
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050168000000000002110100
|GENEINFO=ANO5:203859
|GENE_NAME=ANO5
|GENE_ID=203859
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.22277031C>G
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=NBK114459; 608662.0003
|CLNSIG=5
|CLNCUI=C1969785
|CLNDBN=Limb-girdle muscular dystrophy, type 2L; not provided
|Disease=Limb-girdle muscular dystrophy; not provided
|CLNACC=RCV000002246.3; RCV000082843.1
|Tags=PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK114459:C1969785:611307:206549
}}{{PMID Auto
|PMID=20096397
|Title=Recessive mutations in the putative calcium-activated chloride channel Anoctamin 5 cause proximal LGMD2L and distal MMD3 muscular dystrophies.
|OA=1
}}