ClinVar Miner

Submissions for variant NM_000179.2(MSH6):c.941G>A (p.Ser314Asn) (rs760100983)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000410264 SCV000487815 uncertain significance Hereditary nonpolyposis colorectal cancer type 5 2015-11-17 criteria provided, single submitter clinical testing
Ambry Genetics RCV000576046 SCV000662513 uncertain significance Hereditary cancer-predisposing syndrome 2019-04-04 criteria provided, single submitter clinical testing Insufficient evidence
Color RCV000576046 SCV001350843 uncertain significance Hereditary cancer-predisposing syndrome 2020-03-03 criteria provided, single submitter clinical testing

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