{{Rsnum
|rsid=3888511
|Gene=MT-RNR1
|Chromosome=MT
|position=961
|Orientation=plus
|GMAF=0.01029
|Assembly=GRCh37
|GenomeBuild=37.1
|dbSNPBuild=132
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
}}
{{PMID Auto
|PMID=15286157
|Title=Molecular analysis of the mitochondrial 12S rRNA and tRNASer(UCN) genes in paediatric subjects with non-syndromic hearing loss.
|OA=1
}}

{{ClinVar
|ALT=C,G
|CAF=0.9878; 0.01029; 0.001871
|CHROM=MT
|CLNACC=RCV000035061.1; RCV000010264.1; RCV000035062.1
|CLNALLE=1; 2
|CLNDBN=AllHighlyPenetrant; Deafness, nonsyndromic sensorineural, mitochondrial
|CLNDSDB=MedGen; GeneReviews:GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=CN169374; NBK1422:NBK1434:C3151897:500008:90641
|CLNHGVS=NC_012920.1:m.961T>C; NC_012920.1:m.961T>G
|CLNORIGIN=1
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=561000.0005
|COMMON=1
|Disease=AllHighlyPenetrant; Deafness
|FwdALT=C,G
|FwdREF=T
|REF=T
|RSPOS=961
|Reversed=0
|SAO=1
|SSR=0
|Tags=PM;PMC;SLO;HD;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050168000000100402110100
|WGT=0
|dbSNPBuildID=108
|rsid=3888511
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}