{{Rsnum
|rsid=387906487
|Chromosome=X
|Orientation=plus
|geno1=(-;-)
|geno2=(-;C)
|geno3=(C;C)
|Gene=AMELX
|position=11298246
|Gene_s=AMELX,ARHGAP6
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=X
|CLNACC=RCV000011887.1
|CLNALLE=1
|CLNDBN=AMELOGENESIS IMPERFECTA, TYPE IE
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1845052:301200:88661
|CLNHGVS=NC_000023.10:g.11316366delC
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=300391.0002
|Disease=AMELOGENESIS IMPERFECTA
|FwdREF=C
|REF=AC
|RSPOS=11316362
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050060000000000002110200
|WGT=0
|dbSNPBuildID=137
|rsid=387906487
|GENEINFO=AMELX:265; ARHGAP6:395
|GENE_ID=265; 395
|GENE_NAME=AMELX; ARHGAP6
}}