ClinVar Miner

Submissions for variant NM_000142.5(FGFR3):c.930+10C>T

gnomAD frequency: 0.00014  dbSNP: rs534857289
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Athena Diagnostics RCV000711643 SCV000842029 benign not provided 2017-11-03 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000711643 SCV001092481 benign not provided 2024-01-20 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV000711643 SCV001477686 likely benign not provided 2019-10-24 criteria provided, single submitter clinical testing

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