ClinVar Miner

Submissions for variant NM_000179.3(MSH6):c.2692_2693del (p.Asn897_Pro898insTer)

dbSNP: rs1553414029
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000662902 SCV000785823 likely pathogenic Lynch syndrome 5 2017-12-12 criteria provided, single submitter clinical testing

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