ClinVar Miner

Submissions for variant NM_000535.7(PMS2):c.903+20_903+21del

dbSNP: rs746861817
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000412364 SCV000488621 likely benign Lynch syndrome 4 2016-05-06 criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV000776139 SCV000911129 likely benign Hereditary cancer-predisposing syndrome 2017-11-16 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002058841 SCV002448178 likely benign Hereditary nonpolyposis colorectal neoplasms 2024-08-02 criteria provided, single submitter clinical testing

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