ClinVar Miner

Submissions for variant NM_002160.4(TNC):c.2131+38T>C

gnomAD frequency: 0.56997  dbSNP: rs1755639
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001671993 SCV001888142 benign not provided 2018-11-29 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001838756 SCV002098568 benign Autosomal dominant nonsyndromic hearing loss 56 2021-09-10 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001671993 SCV005315812 benign not provided criteria provided, single submitter not provided

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