ClinVar Miner

Submissions for variant NM_018993.4(RIN2):c.2418C>A (p.Thr806=)

gnomAD frequency: 0.00218  dbSNP: rs114329888
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
GeneDx RCV000862537 SCV000717391 likely benign not provided 2021-12-13 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000862537 SCV001003055 benign not provided 2025-01-27 criteria provided, single submitter clinical testing

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