ClinVar Miner

Submissions for variant NM_000264.5(PTCH1):c.1503+15A>G

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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 RCV005176769 SCV005813771 likely benign Gorlin syndrome 2024-08-14 criteria provided, single submitter clinical testing

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