ClinVar Miner

Submissions for variant NM_007289.4(MME):c.197-15T>G

gnomAD frequency: 0.01943  dbSNP: rs79413638
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
GeneDx RCV001637909 SCV001848824 benign not provided 2019-05-07 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001637909 SCV002399976 benign not provided 2025-02-03 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001637909 SCV005304168 benign not provided criteria provided, single submitter not provided

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