ClinVar Miner

Submissions for variant NM_017662.5(TRPM6):c.2586G>A (p.Val862=)

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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 RCV005182423 SCV005806906 likely benign not provided 2024-08-21 criteria provided, single submitter clinical testing

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