ClinVar Miner

Submissions for variant NM_007289.4(MME):c.161-20A>G

gnomAD frequency: 0.00001  dbSNP: rs780349049
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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 RCV002137318 SCV002420186 likely benign not provided 2021-09-18 criteria provided, single submitter clinical testing

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