{{Rsnum
|rsid=121908116
|Chromosome=1
|Orientation=plus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=EDARADD
|position=236482366
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=EDARADD
}}{{omim
|id=606603
|rsnum=121908116
|variant=0002
}}{{ClinVar
|rsid=121908116
|Reversed=0
|FwdREF=T
|FwdALT=G
|REF=T
|ALT=G
|RSPOS=236482366
|CHROM=1
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000a05000002110100
|GENEINFO=EDARADD:128178
|GENE_NAME=EDARADD
|GENE_ID=128178
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.236482366T>G
|CLNORIGIN=1
|CLNSIG=5
|Tags=PM;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNACC=RCV000004408.1; RCV000055985.1
|CLNDBN=Ectodermal dysplasia 11a, hypohidrotic/hair/tooth type, autosomal dominant; Autosomal dominant hypohidrotic ectodermal dysplasia
|CLNDSDB=MedGen:OMIM:Orphanet:Orphanet; GeneReviews:MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=CN160753:614940:ORPHA1810:ORPHA238468; NBK1112:C1720965:129490:ORPHA1810:ORPHA238468
|CLNSRC=ClinVar; GeneReviews; OMIM Allelic Variant
|CLNSRCID=NM_145861.2:c.365T>G; NBK1112; 606603.0002
|Disease=Ectodermal dysplasia 11a; Autosomal dominant hypohidrotic ectodermal dysplasia
}}