ClinVar Miner

Submissions for variant NM_000249.4(MLH1):c.1314T>C (p.Ala438=)

dbSNP: rs1575537543
Minimum review status: Collection method:
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001484725 SCV001689148 likely benign Hereditary nonpolyposis colorectal neoplasms 2018-02-28 criteria provided, single submitter clinical testing

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