ClinVar Miner

Submissions for variant NM_000455.5(STK11):c.862+8C>T

dbSNP: rs1555738737
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV000583177 SCV000691556 likely benign Hereditary cancer-predisposing syndrome 2016-12-08 criteria provided, single submitter clinical testing
Invitae RCV001489393 SCV001693935 likely benign Peutz-Jeghers syndrome 2023-05-17 criteria provided, single submitter clinical testing

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