ClinVar Miner

Submissions for variant NM_022336.4(EDAR):c.78G>A (p.Ala26=)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003787954 SCV004604799 likely benign Ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominant; Autosomal recessive hypohidrotic ectodermal dysplasia syndrome 2023-06-20 criteria provided, single submitter clinical testing

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