ClinVar Miner

Submissions for variant NM_002361.4(MAG):c.642G>A (p.Arg214=)

dbSNP: rs1279257840
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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 RCV002092329 SCV002324576 likely benign Hereditary spastic paraplegia 75 2021-11-19 criteria provided, single submitter clinical testing

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