ClinVar Miner

Submissions for variant NM_018834.6(MATR3):c.1435-14_1435-11del

gnomAD frequency: 0.00008  dbSNP: rs754942776
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV002170244 SCV002331751 likely benign Amyotrophic lateral sclerosis type 21 2021-08-25 criteria provided, single submitter clinical testing

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