ClinVar Miner

Submissions for variant NM_000455.5(STK11):c.863-5C>T

dbSNP: rs1599928248
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Mendelics RCV000990130 SCV001140942 uncertain significance Peutz-Jeghers syndrome 2019-05-28 criteria provided, single submitter clinical testing
Invitae RCV000990130 SCV001683421 likely benign Peutz-Jeghers syndrome 2021-11-14 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV000990130 SCV002057291 likely benign Peutz-Jeghers syndrome 2021-07-15 criteria provided, single submitter clinical testing

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