ClinVar Miner

Submissions for variant NM_017671.5(FERMT1):c.533-25A>G

gnomAD frequency: 0.14844  dbSNP: rs11087718
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 RCV001676844 SCV001892458 benign not provided 2021-05-12 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001676844 SCV005311710 benign not provided criteria provided, single submitter not provided

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