{{Rsnum
|rsid=28999112
|Gene=ACTG1
|Chromosome=17
|position=81511078
|Orientation=minus
|ReferenceAllele=C
|MissenseAllele=T
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ACTG1
}}[[deafness]]
{{omim
|desc=DEAFNESS, AUTOSOMAL DOMINANT 20
|id=102560
|rsnum=28999112
|variant=0005
}}

{{ClinVar
|rsid=28999112
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=79478104
|CHROM=17
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=ACTG1:71
|GENE_NAME=ACTG1
|GENE_ID=71
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000017.10:g.79478104G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=102560.0005
|CLNSIG=5
|CLNCUI=C1858172
|CLNDBN=Deafness, autosomal dominant 20
|Disease=Deafness
|CLNACC=RCV000019984.26
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1434:C1858172:604717:90635
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}