ClinVar Miner

Submissions for variant NM_144997.7(FLCN):c.259_280del (p.Ser87fs)

dbSNP: rs2544283357
Minimum review status: Collection method:
Minimum conflict level:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV003312377 SCV004009755 pathogenic not provided 2023-04-01 criteria provided, single submitter clinical testing FLCN: PVS1, PM2

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