{{Rsnum
|rsid=267606618
|Gene=BIRC6
|Chromosome=MT
|position=1095
|Orientation=plus
|GMAF=0.0009355
|Assembly=GRCh37.p10
|GenomeBuild=37.5
|dbSNPBuild=138
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}
{{ClinVar
|ALT=C
|CAF=0.9991; 0.0009355
|CHROM=MT
|CLNACC=RCV000010259.1; RCV000010260.1; RCV000010261.1; RCV000035031.1
|CLNALLE=1
|CLNDBN=Aminoglycoside-induced deafness; Deafness, nonsyndromic sensorineural, mitochondrial; Auditory neuropathy; AllHighlyPenetrant
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet; MedGen
|CLNDSDBID=NBK1422:NBK1434:C1838854:580000:168609; NBK1422:NBK1434:C3151897:500008:90641; C1852271; CN169374
|CLNHGVS=NC_012920.1:m.1095T>C
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=561000.0003
|COMMON=0
|Disease=Aminoglycoside-induced deafness; Deafness; Auditory neuropathy; AllHighlyPenetrant
|FwdALT=C
|FwdREF=T
|REF=T
|RSPOS=1095
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=267606618
}}