ClinVar Miner

Submissions for variant NM_000535.7(PMS2):c.706-11T>C

dbSNP: rs1185117521
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV000583138 SCV000691098 likely benign Hereditary cancer-predisposing syndrome 2017-10-02 criteria provided, single submitter clinical testing
Sema4, Sema4 RCV000583138 SCV002530379 uncertain significance Hereditary cancer-predisposing syndrome 2022-01-01 criteria provided, single submitter curation
KCCC/NGS Laboratory, Kuwait Cancer Control Center RCV003316770 SCV004016599 likely benign Lynch syndrome 4 2023-07-07 criteria provided, single submitter clinical testing

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