{{Rsnum
|rsid=267606617
|Chromosome=MT
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=BIRC6
|position=1555
|Assembly=GRCh37.p10
|GenomeBuild=37.5
|dbSNPBuild=138
}}{{ClinVar
|ALT=G
|CHROM=MT
|CLNACC=RCV000010254.4; RCV000010255.4; RCV000010256.4
|CLNALLE=1
|CLNDBN=Aminoglycoside-induced deafness; Deafness, nonsyndromic sensorineural, mitochondrial; Cardiomyopathy, restrictive
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet; MedGen
|CLNDSDBID=NBK1422:NBK1434:C1838854:580000:168609; NBK1422:NBK1434:C3151897:500008:90641; C0007196
|CLNHGVS=NC_012920.1:m.1555A>G
|CLNSIG=5
|CLNSRC=GTR; OMIM Allelic Variant
|CLNSRCID=GTR000500593; 561000.0001
|Disease=Aminoglycoside-induced deafness; Deafness; Cardiomyopathy
|FwdALT=G
|FwdREF=A
|REF=A
|RSPOS=1555
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=267606617
}}