{{Rsnum
|rsid=121912947
|Chromosome=6
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=COL11A2
|position=33171763
|Gene_s=COL11A2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=120290
|rsnum=121912947
|variant=0005
}}{{ClinVar
|rsid=121912947
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=33139540
|CHROM=6
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=COL11A2:1302
|GENE_NAME=COL11A2
|GENE_ID=1302
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000006.11:g.33139540G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=120290.0005
|CLNSIG=5
|CLNCUI=C1866095
|CLNDBN=Deafness, autosomal dominant 13
|Disease=Deafness
|CLNACC=RCV000018662.22
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1434:C1866095:601868:90635
}}