ClinVar Miner

Submissions for variant NM_000455.5(STK11):c.734+20G>C

dbSNP: rs375315233
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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 RCV001183894 SCV001349740 likely benign Hereditary cancer-predisposing syndrome 2019-07-30 criteria provided, single submitter clinical testing
Invitae RCV003507359 SCV004290222 likely benign Peutz-Jeghers syndrome 2023-09-23 criteria provided, single submitter clinical testing

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