{{Rsnum
|rsid=137854439
|Chromosome=8
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=FAM83H
|position=143728081
|Gene_s=FAM83H
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=611927
|variant=0005
|rsnum=137854439
}}{{ClinVar
|ALT=T
|CHROM=8
|CLNACC=RCV000000810.1
|CLNALLE=1
|CLNDBN=Amelogenesis imperfecta, hypocalcification type
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0399376:130900:88661:109471001
|CLNHGVS=NC_000008.10:g.144810251C>T
|CLNORIGIN=1
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=611927.0005
|Disease=Amelogenesis imperfecta
|FwdALT=A
|FwdREF=G
|GENEINFO=FAM83H:286077
|GENE_ID=286077
|GENE_NAME=FAM83H
|REF=C
|RSPOS=144810251
|Reversed=1
|SAO=1
|SSR=0
|Tags=RV;PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=133
|rsid=137854439
}}