ClinVar Miner

Submissions for variant NM_007289.4(MME):c.161-13C>T

dbSNP: rs1388013925
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002203196 SCV002484153 likely benign not provided 2021-02-21 criteria provided, single submitter clinical testing

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