ClinVar Miner

Submissions for variant NM_205836.3(FBXO38):c.198A>G (p.Leu66=)

gnomAD frequency: 0.01529  dbSNP: rs74863106
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 RCV002232387 SCV000653620 benign Distal hereditary motor neuropathy type 2 2025-02-03 criteria provided, single submitter clinical testing
GeneDx RCV001644659 SCV001857432 benign not provided 2021-04-17 criteria provided, single submitter clinical testing

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