ClinVar Miner

Submissions for variant NM_002184.4(IL6ST):c.1299C>T (p.Phe433=)

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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 RCV003059767 SCV003354442 likely benign not provided 2022-06-01 criteria provided, single submitter clinical testing

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