ClinVar Miner

Submissions for variant NM_000455.5(STK11):c.975C>T (p.Ser325=)

dbSNP: rs1599929360
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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 RCV001434613 SCV001637423 likely benign Peutz-Jeghers syndrome 2018-10-26 criteria provided, single submitter clinical testing

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