ClinVar Miner

Submissions for variant NM_018993.4(RIN2):c.2220C>T (p.Ser740=)

gnomAD frequency: 0.00080  dbSNP: rs146810222
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000863343 SCV001003989 benign not provided 2024-10-29 criteria provided, single submitter clinical testing
GeneDx RCV000863343 SCV001805027 likely benign not provided 2021-01-13 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV000863343 SCV005207432 likely benign not provided criteria provided, single submitter not provided

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