ClinVar Miner

Submissions for variant NM_001371986.1(UNC80):c.7368A>G (p.Thr2456=)

gnomAD frequency: 0.00001  dbSNP: rs908179337
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002110111 SCV002431430 likely benign not provided 2024-02-08 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV002110111 SCV005258257 likely benign not provided criteria provided, single submitter not provided

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