ClinVar Miner

Submissions for variant NM_002439.5(MSH3):c.1028-11ATT[2]

dbSNP: rs2112815891
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001418170 SCV001620394 likely benign not provided 2023-08-23 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV005038214 SCV005673171 likely pathogenic Endometrial carcinoma; Familial adenomatous polyposis 4 2024-06-16 criteria provided, single submitter clinical testing

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