ClinVar Miner

Submissions for variant NM_000179.3(MSH6):c.3647-35_3647-34insTTTGTTCTAATTCCTTT

dbSNP: rs397515292
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV000030268 SCV000052935 benign Lynch syndrome 2011-08-18 criteria provided, single submitter curation Converted during submission to Benign.

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