ClinVar Miner

Submissions for variant NM_002016.2(FLG):c.9315C>T (p.Tyr3105=)

dbSNP: rs200815866
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 RCV001618881 SCV001844379 benign not provided 2021-06-03 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV001618881 SCV004124733 likely benign not provided 2023-02-01 criteria provided, single submitter clinical testing FLG: BP4, BS2

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