ClinVar Miner

Submissions for variant NM_017999.5(RNF31):c.556-5T>C

gnomAD frequency: 0.00001  dbSNP: rs369056177
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 RCV002002425 SCV002228709 likely benign not provided 2024-11-28 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV002002425 SCV005218975 likely benign not provided criteria provided, single submitter not provided

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