ClinVar Miner

Submissions for variant NM_007289.4(MME):c.1189-4G>A

dbSNP: rs182602615
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002071960 SCV002401704 benign not provided 2024-12-26 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV002071960 SCV002497232 uncertain significance not provided 2022-02-01 criteria provided, single submitter clinical testing
Institute of Human Genetics, University of Wuerzburg RCV001541902 SCV001760546 uncertain significance Peripheral neuropathy no assertion criteria provided clinical testing

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