ClinVar Miner

Submissions for variant NM_001190274.2(FBXO11):c.123C>G (p.Pro41=)

gnomAD frequency: 0.00001  dbSNP: rs1193215846
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002049293 SCV002108255 likely benign not provided 2024-12-22 criteria provided, single submitter clinical testing

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