ClinVar Miner

Submissions for variant NM_001281492.1(MSH6):c.3412-43dup (rs34154602)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
International Society for Gastrointestinal Hereditary Tumours (InSiGHT) RCV000074935 SCV000108148 no known pathogenicity Lynch syndrome 2013-09-05 reviewed by expert panel research MAF >1%
Mayo Clinic Genetic Testing Laboratories,Mayo Clinic RCV000201998 SCV000257281 benign not specified no assertion criteria provided research

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