ClinVar Miner

Submissions for variant NM_000535.7(PMS2):c.23+6C>T

dbSNP: rs779104357
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000410086 SCV000489246 likely benign Lynch syndrome 4 2016-09-07 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001072072 SCV001237415 likely benign Hereditary nonpolyposis colorectal neoplasms 2024-12-08 criteria provided, single submitter clinical testing
Myriad Genetics, Inc. RCV000410086 SCV004019747 likely benign Lynch syndrome 4 2023-04-03 criteria provided, single submitter clinical testing This variant is considered likely benign. This variant is intronic and is not expected to impact mRNA splicing.

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