ClinVar Miner

Submissions for variant NM_000455.4(STK11):c.1128G>A (p.Glu376=) (rs747018506)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000163509 SCV000214067 likely benign Hereditary cancer-predisposing syndrome 2015-03-10 criteria provided, single submitter clinical testing
Invitae RCV000197392 SCV000253244 likely benign Peutz-Jeghers syndrome 2017-08-18 criteria provided, single submitter clinical testing
Color RCV000163509 SCV000686591 likely benign Hereditary cancer-predisposing syndrome 2017-03-07 criteria provided, single submitter clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000759353 SCV000888636 likely benign not provided 2018-04-10 criteria provided, single submitter clinical testing

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