{{Rsnum
|rsid=137854441
|Chromosome=8
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=FAM83H
|position=143728053
|Gene_s=FAM83H
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=611927
|variant=0007
|rsnum=137854441
}}{{ClinVar
|ALT=A
|CHROM=8
|CLNACC=RCV000000812.1
|CLNALLE=1
|CLNDBN=Amelogenesis imperfecta, hypocalcification type
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0399376:130900:88661:109471001
|CLNHGVS=NC_000008.10:g.144810223G>A
|CLNORIGIN=1
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=611927.0007
|Disease=Amelogenesis imperfecta
|FwdALT=T
|FwdREF=C
|GENEINFO=FAM83H:286077
|GENE_ID=286077
|GENE_NAME=FAM83H
|REF=G
|RSPOS=144810223
|Reversed=1
|SAO=1
|SSR=0
|Tags=RV;PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=133
|rsid=137854441
}}