ClinVar Miner

Submissions for variant NM_145861.4(EDARADD):c.161-6del

dbSNP: rs555177993
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001718265 SCV001944696 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Invitae RCV003771865 SCV004573840 benign Ectodermal dysplasia 11A, hypohidrotic/hair/tooth type, autosomal dominant; Ectodermal dysplasia 11B, hypohidrotic/hair/tooth type, autosomal recessive 2023-05-27 criteria provided, single submitter clinical testing

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