ClinVar Miner

Submissions for variant NM_002160.4(TNC):c.2620A>G (p.Ile874Val)

gnomAD frequency: 0.01101  dbSNP: rs61737743
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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Pediatric Genomic Medicine, Children's Mercy Hospital and Clinics RCV000514304 SCV000610359 likely benign not provided 2017-07-24 criteria provided, single submitter clinical testing
Invitae RCV000514304 SCV001037709 benign not provided 2019-12-31 criteria provided, single submitter clinical testing
Athena Diagnostics Inc RCV000514304 SCV001146209 benign not provided 2018-11-14 criteria provided, single submitter clinical testing
GeneDx RCV000514304 SCV001865808 benign not provided 2020-01-06 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002270612 SCV002554472 benign Autosomal dominant nonsyndromic hearing loss 56 2022-03-15 criteria provided, single submitter clinical testing

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