ClinVar Miner

Submissions for variant NM_000455.5(STK11):c.930G>C (p.Arg310=)

dbSNP: rs2080795732
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Sema4, Sema4 RCV002255911 SCV002526962 likely benign Hereditary cancer-predisposing syndrome 2021-10-29 criteria provided, single submitter curation
Invitae RCV003094223 SCV003032453 likely benign Peutz-Jeghers syndrome 2022-09-25 criteria provided, single submitter clinical testing

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