ClinVar Miner

Submissions for variant NM_000455.5(STK11):c.734+11C>T

gnomAD frequency: 0.00004  dbSNP: rs773604294
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001722202 SCV000279181 likely benign not provided 2020-09-15 criteria provided, single submitter clinical testing
Counsyl RCV000410618 SCV000489295 likely benign Peutz-Jeghers syndrome 2016-09-13 criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV000771477 SCV000903936 likely benign Hereditary cancer-predisposing syndrome 2016-10-12 criteria provided, single submitter clinical testing
Invitae RCV000410618 SCV002380137 likely benign Peutz-Jeghers syndrome 2024-01-17 criteria provided, single submitter clinical testing

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