{{Rsnum
|rsid=132630314
|Chromosome=X
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=EDA
|position=69957097
|Gene_s=EDA
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=300451
|variant=0007
|rsnum=132630314
}}{{ClinVar
|rsid=132630314
|Reversed=0
|FwdREF=G
|FwdALT=A,T
|REF=G
|ALT=A,T
|RSPOS=69176947
|CHROM=X
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=EDA:1896
|GENE_NAME=EDA
|GENE_ID=1896
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000023.10:g.69176947G>A; NC_000023.10:g.69176947G>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=300451.0007
|CLNSIG=5
|CLNCUI=CN069564
|CLNDBN=Hypohidrotic X-linked ectodermal dysplasia; Hypohidrotic ectodermal dysplasia
|Disease=Hypohidrotic X-linked ectodermal dysplasia; Hypohidrotic ectodermal dysplasia
|CLNACC=RCV000032612.1; RCV000037171.1; RCV000037172.1
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet:SNOMED_CT; GeneReviews:MedGen
|CLNDSDBID=NBK1112:C0162359:305100:181:238468:239007005; NBK1112:CN072978
}}