ClinVar Miner

Submissions for variant NM_018834.6(MATR3):c.1603-17T>C

dbSNP: rs199789148
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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 RCV002127242 SCV002403242 benign Amyotrophic lateral sclerosis type 21 2023-11-18 criteria provided, single submitter clinical testing

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