ClinVar Miner

Submissions for variant NM_018993.4(RIN2):c.463+12T>C

gnomAD frequency: 0.00218  dbSNP: rs184313079
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 RCV001707844 SCV000732537 likely benign not provided 2018-03-26 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001707844 SCV002405440 benign not provided 2025-01-15 criteria provided, single submitter clinical testing

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