ClinVar Miner

Submissions for variant NM_000455.5(STK11):c.734+8C>T

dbSNP: rs561655034
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000921423 SCV001066825 likely benign Peutz-Jeghers syndrome 2021-09-22 criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV001181032 SCV001346087 likely benign Hereditary cancer-predisposing syndrome 2019-03-04 criteria provided, single submitter clinical testing

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