ClinVar Miner

Submissions for variant NM_000535.7(PMS2):c.1335C>T (p.Ser445=)

dbSNP: rs1562634446
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV000777533 SCV000913396 likely benign Hereditary cancer-predisposing syndrome 2018-02-12 criteria provided, single submitter clinical testing
Invitae RCV002535621 SCV003232598 likely benign Hereditary nonpolyposis colorectal neoplasms 2022-09-05 criteria provided, single submitter clinical testing

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