ClinVar Miner

Submissions for variant NM_000249.4(MLH1):c.678-14C>A

dbSNP: rs773646445
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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 RCV002114298 SCV002445588 likely benign Hereditary nonpolyposis colorectal neoplasms 2023-01-24 criteria provided, single submitter clinical testing
CHEO Genetics Diagnostic Laboratory, Children's Hospital of Eastern Ontario RCV003150486 SCV003838208 likely benign Breast and/or ovarian cancer 2022-02-16 criteria provided, single submitter clinical testing

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