ClinVar Miner

Submissions for variant NM_000179.3(MSH6):c.3837_3843del (p.Ser1279fs)

dbSNP: rs1553333370
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ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000662746 SCV000785526 likely pathogenic Lynch syndrome 5 2017-09-11 criteria provided, single submitter clinical testing

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