{{Rsnum
|rsid=387907215
|Chromosome=17
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=FAM20A
|position=68542796
|Gene_s=FAM20A,PRKAR1A
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=17
|CLNACC=RCV000029154.1
|CLNALLE=1
|CLNDBN=Amelogenesis imperfecta and gingival fibromatosis syndrome
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C3280276:614253:171836
|CLNHGVS=NC_000017.10:g.66538937G>A
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=611062.0006
|Disease=Amelogenesis imperfecta and gingival fibromatosis syndrome
|FwdALT=T
|FwdREF=C
|REF=G
|RSPOS=66538937
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=387907215
|GENEINFO=PRKAR1A:5573; FAM20A:54757
|GENE_ID=5573; 54757
|GENE_NAME=PRKAR1A; FAM20A
}}