ClinVar Miner

Submissions for variant NM_018993.4(RIN2):c.1427C>G (p.Pro476Arg)

gnomAD frequency: 0.00165  dbSNP: rs35142632
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV000194872 SCV000248721 uncertain significance not specified 2015-03-16 criteria provided, single submitter clinical testing
GeneDx RCV000828502 SCV000970194 likely benign not provided 2020-05-22 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000828502 SCV001001565 benign not provided 2023-11-27 criteria provided, single submitter clinical testing

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