ClinVar Miner

Submissions for variant NM_016156.6(MTMR2):c.1218A>C (p.Val406=)

dbSNP: rs2135426567
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV001726854 SCV001961304 likely benign not provided 2021-08-01 criteria provided, single submitter clinical testing

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