ClinVar Miner

Submissions for variant NM_000535.7(PMS2):c.164-6T>C

dbSNP: rs1060504837
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV002230862 SCV000562209 likely benign Hereditary nonpolyposis colorectal neoplasms 2023-01-26 criteria provided, single submitter clinical testing

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