ClinVar Miner

Submissions for variant NM_002361.4(MAG):c.712+19GGGGCGGGGT[4]

dbSNP: rs773009758
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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 RCV002123852 SCV002442512 likely benign Hereditary spastic paraplegia 75 2023-12-18 criteria provided, single submitter clinical testing

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