ClinVar Miner

Submissions for variant NM_000142.5(FGFR3):c.2259C>T (p.Thr753=)

gnomAD frequency: 0.00015  dbSNP: rs146662137
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
Athena Diagnostics RCV000711637 SCV000842023 benign not provided 2018-01-26 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000711637 SCV001118436 likely benign not provided 2023-10-22 criteria provided, single submitter clinical testing

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