{{Rsnum
|rsid=104894737
|Chromosome=X
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=AMELX
|position=11294790
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=AMELX,ARHGAP6
}}{{omim
|id=300391
|rsnum=104894737
|variant=0010
}}{{ClinVar
|rsid=104894737
|Reversed=0
|FwdREF=T
|FwdALT=C
|REF=T
|ALT=C
|RSPOS=11312910
|CHROM=X
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=AMELX:265; ARHGAP6:395
|GENE_NAME=AMELX; ARHGAP6
|GENE_ID=265; 395
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.11312910T>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=300391.0010
|CLNSIG=5
|CLNCUI=C1845052
|CLNDBN=AMELOGENESIS IMPERFECTA, TYPE IE
|Disease=AMELOGENESIS IMPERFECTA
|CLNACC=RCV000011895.4
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1845052:301200:88661
}}