{{Rsnum
|rsid=397514736
|Chromosome=11
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=ANO5
|position=22259652
|Gene_s=ANO5
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=11
|CLNACC=RCV000054502.1
|CLNALLE=1
|CLNDBN=Osteogenesis imperfecta Levin type
|CLNDSDB=GeneReviews:MedGen:OMIM
|CLNDSDBID=NBK114459:C1833736:166260
|CLNHGVS=NC_000011.9:g.22281198C>T
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=608662.0009
|Disease=Osteogenesis imperfecta Levin type
|FwdALT=T
|FwdREF=C
|GENEINFO=ANO5:203859
|GENE_ID=203859
|GENE_NAME=ANO5
|REF=C
|RSPOS=22281198
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=136
|rsid=397514736
}}