ClinVar Miner

Submissions for variant NM_000455.5(STK11):c.1108+1_1108+5dup

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Fulgent Genetics, Fulgent Genetics RCV005026358 SCV005655485 uncertain significance Peutz-Jeghers syndrome; Melanoma, cutaneous malignant, susceptibility to, 1; Familial pancreatic carcinoma; Germ cell tumor of testis 2024-05-21 criteria provided, single submitter clinical testing

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