ClinVar Miner

Submissions for variant NM_002160.4(TNC):c.276G>A (p.Val92=)

gnomAD frequency: 0.47973  dbSNP: rs944510
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001654134 SCV001863826 benign not provided 2018-11-29 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001838731 SCV002098575 benign Autosomal dominant nonsyndromic hearing loss 56 2021-09-10 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001654134 SCV005317210 benign not provided criteria provided, single submitter not provided

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