ClinVar Miner

Submissions for variant NM_001453.3(FOXC1):c.18C>G (p.Ser6=)

dbSNP: rs1363320651
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002218984 SCV002363378 likely benign Axenfeld-Rieger syndrome type 3 2022-01-15 criteria provided, single submitter clinical testing

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