ClinVar Miner

Submissions for variant NM_145861.4(EDARADD):c.358G>C (p.Asp120His)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Fulgent Genetics, Fulgent Genetics RCV005010113 SCV005639608 uncertain significance Ectodermal dysplasia 11A, hypohidrotic/hair/tooth type, autosomal dominant; Ectodermal dysplasia 11B, hypohidrotic/hair/tooth type, autosomal recessive 2024-04-07 criteria provided, single submitter clinical testing

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