ClinVar Miner

Submissions for variant NM_000455.5(STK11):c.465-20C>T

gnomAD frequency: 0.00003  dbSNP: rs768282654
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000426537 SCV000528755 likely benign not specified 2017-04-24 criteria provided, single submitter clinical testing This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.
Color Diagnostics, LLC DBA Color Health RCV000579993 SCV000686659 likely benign Hereditary cancer-predisposing syndrome 2017-01-12 criteria provided, single submitter clinical testing
Invitae RCV002063370 SCV002482226 likely benign Peutz-Jeghers syndrome 2024-01-25 criteria provided, single submitter clinical testing

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