ClinVar Miner

Submissions for variant NM_002361.4(MAG):c.633C>T (p.Asn211=)

gnomAD frequency: 0.00019  dbSNP: rs373301414
Minimum review status: Collection method:
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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 RCV002065805 SCV002468512 likely benign Hereditary spastic paraplegia 75 2022-08-16 criteria provided, single submitter clinical testing

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