ClinVar Miner

Submissions for variant NM_000455.4(STK11):c.42G>A (p.Glu14=) (rs758769888)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000760082 SCV000253254 likely benign not provided 2019-02-14 criteria provided, single submitter clinical testing
Ambry Genetics RCV000572557 SCV000664338 likely benign Hereditary cancer-predisposing syndrome 2015-05-10 criteria provided, single submitter clinical testing
Color RCV000572557 SCV000686645 likely benign Hereditary cancer-predisposing syndrome 2017-01-17 criteria provided, single submitter clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000760082 SCV000889858 benign not provided 2018-03-02 criteria provided, single submitter clinical testing

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