ClinVar Miner

Submissions for variant NM_000455.5(STK11):c.920+7_920+8delinsCA

dbSNP: rs1057517545
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000412453 SCV000488140 uncertain significance Peutz-Jeghers syndrome 2016-01-06 criteria provided, single submitter clinical testing
Invitae RCV000412453 SCV002336856 likely benign Peutz-Jeghers syndrome 2023-03-03 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV000412453 SCV004017948 likely benign Peutz-Jeghers syndrome 2023-04-12 criteria provided, single submitter clinical testing This variant is considered likely benign. This variant is intronic and is not expected to impact mRNA splicing.
Color Diagnostics, LLC DBA Color Health RCV003584591 SCV004362408 likely benign Hereditary cancer-predisposing syndrome 2022-11-16 criteria provided, single submitter clinical testing

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