ClinVar Miner

Submissions for variant NM_015450.3(POT1):c.702+8_702+9delinsTG

dbSNP: rs36069303
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000542608 SCV000655200 benign Tumor predisposition syndrome 3 2025-02-04 criteria provided, single submitter clinical testing
Institute of Human Genetics, University of Leipzig Medical Center RCV001262967 SCV001441031 likely benign Breast carcinoma 2019-01-01 criteria provided, single submitter clinical testing

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