ClinVar Miner

Submissions for variant NM_000179.2(MSH6):c.615A>G (p.Glu205=) (rs1334827373)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000589743 SCV000624985 likely benign not provided 2018-12-25 criteria provided, single submitter clinical testing
Integrated Genetics/Laboratory Corporation of America RCV000855559 SCV000695917 likely benign not specified 2019-08-29 criteria provided, single submitter clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000589743 SCV000888293 likely benign not provided 2019-04-09 criteria provided, single submitter clinical testing

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