ClinVar Miner

Submissions for variant NM_000249.4(MLH1):c.186A>G (p.Gln62=)

dbSNP: rs1559506261
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Mendelics RCV000987144 SCV001136367 uncertain significance Colorectal cancer, hereditary nonpolyposis, type 2 2019-05-28 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001444066 SCV001647059 likely benign Hereditary nonpolyposis colorectal neoplasms 2018-11-06 criteria provided, single submitter clinical testing

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