{{Rsnum
|rsid=260630
|Gene=EDAR
|Chromosome=2
|position=108910917
|Orientation=minus
|GMAF=0.0652
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=EDAR
}}{{Venter SNP
|rsid=260630
|allele=G
|frequency=
|uid=1103658181260
|type=heterozygous_SNP
|hugo=EDAR
|ensembl gene=ENSG00000135960
|ensembl transcript=ENST00000376651
|sift=TOLERATED
|disease=Defects in EDAR are a cause of hypohidrotic ectodermal dysplasia (HED) (MIM:129490, 224900); also known as anhidrotic ectodermal dysplasia (EDA). Inheritance can be autosomal dominant or recessive. HED is characterized by sparse hair (atrichosis or hypotrichosis), abnormal or missing teeth and the inability to sweat due to the absence of sweat glands.
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}