ClinVar Miner

Submissions for variant NM_018834.6(MATR3):c.1017-4C>T

dbSNP: rs1035772952
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001498510 SCV001703260 likely benign Amyotrophic lateral sclerosis type 21 2020-06-02 criteria provided, single submitter clinical testing

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