ClinVar Miner

Submissions for variant NM_000141.5(FGFR2):c.864_881del (p.Ile288_Val294delinsMet)

dbSNP: rs886037837
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ClinVar Staff, National Center for Biotechnology Information (NCBI) RCV000240846 SCV000292256 pathogenic Pfeiffer syndrome no assertion criteria provided literature only

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