{{Rsnum
|rsid=387907149
|Chromosome=19
|Orientation=plus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=CEACAM16
|position=44704053
|Gene_s=CEACAM16
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=C
|CHROM=19
|CLNACC=RCV000024237.1
|CLNALLE=1
|CLNDBN=Deafness, autosomal dominant 4b
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C3281297:614614:90635
|CLNHGVS=NC_000019.9:g.45207323A>C
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=614591.0001
|Disease=Deafness
|FwdALT=C
|FwdREF=A
|REF=A
|RSPOS=45207323
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=387907149
|GENEINFO=CEACAM16:388551
|GENE_ID=388551
|GENE_NAME=CEACAM16
}}