ClinVar Miner

List of variants reported as uncertain significance for Ectodermal dysplasia 10B, hypohidrotic/hair/tooth type, autosomal recessive; Ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominant

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NC_000002.11:g.(?_109336043)_(109579739_?)dup
NC_000002.11:g.(?_109367964)_(109579739_?)dup
NM_022336.4(EDAR):c.328G>A (p.Asp110Asn)	rs1574385383

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