ClinVar Miner

Submissions for variant NM_000455.4(STK11):c.306G>C (p.Leu102=) (rs370130178)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000205991 SCV000260112 likely benign not provided 2015-09-03 criteria provided, single submitter clinical testing
Ambry Genetics RCV000221681 SCV000275286 likely benign Hereditary cancer-predisposing syndrome 2015-04-28 criteria provided, single submitter clinical testing

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