{{Rsnum
|rsid=121434467
|Gene=ADAM11
|Chromosome=MT
|position=4295
|Orientation=plus
|GMAF=0.001871
|Assembly=GRCh37.p10
|GenomeBuild=37.5
|dbSNPBuild=138
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}
{{ClinVar
|ALT=G
|CAF=0.9981; 0.001871
|CHROM=MT
|CLNACC=RCV000010226.1; RCV000022900.1
|CLNALLE=1
|CLNDBN=Cardiomyopathy, familial hypertrophic; Deafness, nonsyndromic sensorineural, mitochondrial
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1422:NBK1434:C3151897:500008:90641
|CLNHGVS=NC_012920.1:m.4295A>G
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=590045.0003
|COMMON=0
|Disease=Cardiomyopathy; Deafness
|FwdALT=G
|FwdREF=A
|REF=A
|RSPOS=4295
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=132
|rsid=121434467
}}