{{Rsnum
|rsid=137854443
|Chromosome=8
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=FAM83H
|position=143727381
|Gene_s=FAM83H
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=611927
|variant=0009
|rsnum=137854443
}}{{ClinVar
|ALT=A
|CHROM=8
|CLNACC=RCV000000814.1
|CLNALLE=1
|CLNDBN=AMELOGENESIS IMPERFECTA, TYPE III, LOCALIZED
|CLNHGVS=NC_000008.10:g.144809551C>A
|CLNORIGIN=1
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=611927.0009
|Disease=AMELOGENESIS IMPERFECTA
|FwdALT=T
|FwdREF=G
|GENEINFO=FAM83H:286077
|GENE_ID=286077
|GENE_NAME=FAM83H
|REF=C
|RSPOS=144809551
|Reversed=1
|SAO=1
|SSR=0
|Tags=RV;PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=133
|rsid=137854443
}}