{{Rsnum
|rsid=121908109
|Chromosome=4
|Orientation=plus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=ENAM
|position=70631882
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ENAM
}}{{omim
|id=606585
|rsnum=121908109
|variant=0002
}}{{ClinVar
|rsid=121908109
|Reversed=0
|FwdREF=A
|FwdALT=T
|REF=A
|ALT=T
|RSPOS=71497599
|CHROM=4
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=ENAM:10117
|GENE_NAME=ENAM
|GENE_ID=10117
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000004.11:g.71497599A>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=606585.0002
|CLNSIG=5
|CLNCUI=C0399368
|CLNDBN=Amelogenesis imperfecta - hypoplastic autosomal dominant - local
|Disease=Amelogenesis imperfecta - hypoplastic autosomal dominant - local
|CLNACC=RCV000004459.1
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0399368:104500:88661:234961008
}}