{{Rsnum
|rsid=121908406
|Chromosome=5
|Orientation=minus
|geno1=(-;-)
|geno2=(-;TCC)
|geno3=(TCC;TCC)
|Gene=ANKH
|position=14716722
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ANKH,IGKV2-28
}}{{omim
|id=605145
|rsnum=121908406
|variant=0005
}}{{ClinVar
|rsid=121908406
|Reversed=1
|FwdREF=CCT
|FwdALT=
|REF=AGGA
|ALT=A
|RSPOS=14716830
|CHROM=5
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110200
|GENEINFO=LOC100130744:100130744; ANKH:56172
|GENE_NAME=LOC100130744; ANKH
|GENE_ID=100130744; 56172
|WGT=0
|VC=DIV
|CLNALLE=1
|CLNHGVS=NC_000005.9:g.14716831_14716833delGGA
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=605145.0005
|CLNSIG=5
|CLNCUI=C1852502
|CLNDBN=Craniometaphyseal dysplasia, autosomal dominant
|Disease=Craniometaphyseal dysplasia
|CLNACC=RCV000005504.1
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1461:C1852502:123000:1522
}}