ClinVar Miner

Submissions for variant NM_022336.4(EDAR):c.655+30T>C

gnomAD frequency: 0.90817  dbSNP: rs260630
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genomic Research Center, Shahid Beheshti University of Medical Sciences RCV000143984 SCV000188870 benign not provided 2020-05-03 criteria provided, single submitter clinical testing
GeneDx RCV000143984 SCV001846047 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001657825 SCV001875919 benign Ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominant 2021-07-30 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001657824 SCV001875920 benign Ectodermal dysplasia 10B, hypohidrotic/hair/tooth type, autosomal recessive 2021-07-30 criteria provided, single submitter clinical testing

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