ClinVar Miner

Submissions for variant NM_000455.5(STK11):c.375-16_375-15delinsCC

dbSNP: rs2145422079
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV002146817 SCV002415859 likely benign Peutz-Jeghers syndrome 2021-09-07 criteria provided, single submitter clinical testing

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