{{Rsnum
|rsid = 28939080
|Gene = ANKH
|geno1 = (A;A)
|geno2 = (A;G)
|geno3 = (G;G)
|Orientation=minus
|ReferenceAllele=G
|MissenseAllele=A
|Chromosome=5
|position=14713644
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ANKH,IGKV2-28
}}{{omim
|desc=CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT
|id=605145
|rsnum=28939080
|variant=0002
}}

{{ClinVar
|rsid=28939080
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=14713753
|CHROM=5
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=LOC100130744:100130744; ANKH:56172
|GENE_NAME=LOC100130744; ANKH
|GENE_ID=100130744; 56172
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000005.9:g.14713753C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=605145.0002
|CLNSIG=5
|CLNCUI=C1852502
|CLNDBN=Craniometaphyseal dysplasia, autosomal dominant; Chondrocalcinosis 2
|Disease=Craniometaphyseal dysplasia; Chondrocalcinosis 2
|CLNACC=RCV000005502.1; RCV000032998.1
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet; MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1461:C1852502:123000:1522; C0856830:118600:1416
}}

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