{{Rsnum
|rsid=144411158
|Gene=FAM20A
|Chromosome=17
|position=68555742
|Orientation=plus
|GMAF=0.0004591
|Gene_s=FAM20A
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ClinVar
|ALT=A
|CAF=0.9995; 0.0004591
|CHROM=17
|CLNACC=RCV000023864.1
|CLNALLE=1
|CLNDBN=Amelogenesis imperfecta and gingival fibromatosis syndrome
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C3280276:614253:171836
|CLNHGVS=NC_000017.10:g.66551883G>A
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=611062.0001
|COMMON=0
|Disease=Amelogenesis imperfecta and gingival fibromatosis syndrome
|FwdALT=A
|FwdREF=G
|GENEINFO=FAM20A:54757
|GENE_ID=54757
|GENE_NAME=FAM20A
|REF=G
|RSPOS=66551883
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;KGPhase1;KGPROD;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000016110100
|WGT=0
|dbSNPBuildID=134
|rsid=144411158
}}