ClinVar Miner

Submissions for variant NM_000535.7(PMS2):c.2275+12_2275+15del

dbSNP: rs758812244
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001714355 SCV001944560 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002073354 SCV002336072 likely benign Hereditary nonpolyposis colorectal neoplasms 2024-01-28 criteria provided, single submitter clinical testing
Sema4, Sema4 RCV002255687 SCV002530280 likely benign Hereditary cancer-predisposing syndrome 2021-01-26 criteria provided, single submitter curation

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