ClinVar Miner

Submissions for variant NM_002439.5(MSH3):c.1365C>G (p.Val455=)

dbSNP: rs771995449
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 RCV002079289 SCV002426482 likely benign not provided 2024-08-01 criteria provided, single submitter clinical testing

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