ClinVar Miner

Submissions for variant NM_002439.5(MSH3):c.793-3dup

dbSNP: rs754475791
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
Labcorp Genetics (formerly Invitae), Labcorp RCV001510305 SCV001717309 benign not provided 2020-02-03 criteria provided, single submitter clinical testing

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