ClinVar Miner

Submissions for variant NM_005612.5(REST):c.898+15C>T

gnomAD frequency: 0.00026  dbSNP: rs148949163
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002098145 SCV002389552 benign not provided 2023-03-10 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002507965 SCV002804391 likely benign Autosomal dominant nonsyndromic hearing loss 27; Wilms tumor 6; Fibromatosis, gingival, 5 2021-12-20 criteria provided, single submitter clinical testing

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