ClinVar Miner

Submissions for variant NM_000455.5(STK11):c.464+20del

dbSNP: rs730881960
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Total submissions: 6
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000160971 SCV000211680 benign Hereditary cancer-predisposing syndrome 2014-08-21 criteria provided, single submitter clinical testing The variant is found in HEREDICANCER,BR-OV-HEREDIC panel(s).
Counsyl RCV000410927 SCV000489224 likely benign Peutz-Jeghers syndrome 2016-09-06 criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV000160971 SCV000686653 benign Hereditary cancer-predisposing syndrome 2016-08-31 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV000679318 SCV000806079 benign not specified 2017-12-20 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV000410927 SCV002057409 likely benign Peutz-Jeghers syndrome 2021-07-15 criteria provided, single submitter clinical testing
Invitae RCV000410927 SCV002425246 benign Peutz-Jeghers syndrome 2024-02-01 criteria provided, single submitter clinical testing

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