ClinVar Miner

Submissions for variant NM_000141.5(FGFR2):c.1987-5T>G

gnomAD frequency: 0.00006  dbSNP: rs778413728
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000923800 SCV001069295 likely benign FGFR2-related craniosynostosis 2022-08-06 criteria provided, single submitter clinical testing

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