ClinVar Miner

Submissions for variant NM_000455.5(STK11):c.921-6T>C

dbSNP: rs759049461
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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 RCV001401980 SCV001603820 likely benign Peutz-Jeghers syndrome 2020-10-06 criteria provided, single submitter clinical testing

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