ClinVar Miner

Submissions for variant NM_000455.5(STK11):c.1113G>A (p.Gln371=)

dbSNP: rs587780714
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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 RCV001185727 SCV001351985 likely benign Hereditary cancer-predisposing syndrome 2019-08-12 criteria provided, single submitter clinical testing
Invitae RCV000123053 SCV000166348 likely benign Peutz-Jeghers syndrome 2014-11-06 no assertion criteria provided clinical testing

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