{{Rsnum
|rsid=267606619
|Chromosome=MT
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=BIRC6
|position=1494
|Assembly=GRCh37.p10
|GenomeBuild=37.5
|dbSNPBuild=138
}}{{ClinVar
|ALT=T
|CHROM=MT
|CLNACC=RCV000010262.2; RCV000010263.2
|CLNALLE=1
|CLNDBN=Aminoglycoside-induced deafness; Deafness, nonsyndromic sensorineural, mitochondrial
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1422:NBK1434:C1838854:580000:168609; NBK1422:NBK1434:C3151897:500008:90641
|CLNHGVS=NC_012920.1:m.1494C>T
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=561000.0004
|Disease=Aminoglycoside-induced deafness; Deafness
|FwdALT=T
|FwdREF=C
|REF=C
|RSPOS=1494
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=267606619
}}