ClinVar Miner

Submissions for variant NM_018834.6(MATR3):c.1129+7A>G

dbSNP: rs1477606021
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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 RCV001400282 SCV001602086 likely benign Amyotrophic lateral sclerosis type 21 2022-07-06 criteria provided, single submitter clinical testing

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