ClinVar Miner

Submissions for variant NM_002160.4(TNC):c.2562C>T (p.Asp854=)

gnomAD frequency: 0.02872  dbSNP: rs61739209
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Athena Diagnostics RCV000993339 SCV001146208 benign not provided 2019-06-26 criteria provided, single submitter clinical testing
GeneDx RCV000993339 SCV001756156 benign not provided 2019-12-09 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001838649 SCV002098566 benign Autosomal dominant nonsyndromic hearing loss 56 2021-09-10 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV000993339 SCV005316473 benign not provided criteria provided, single submitter not provided

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