ClinVar Miner

Submissions for variant NM_000535.7(PMS2):c.1145-7T>G

dbSNP: rs1554298099
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000630369 SCV000751325 likely benign Hereditary nonpolyposis colorectal neoplasms 2021-05-20 criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV003584683 SCV004359631 likely benign Hereditary cancer-predisposing syndrome 2022-02-16 criteria provided, single submitter clinical testing

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