ClinVar Miner

Submissions for variant NM_002361.4(MAG):c.1140G>A (p.Pro380=)

gnomAD frequency: 0.00011  dbSNP: rs200135379
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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 RCV000952328 SCV001098823 benign Hereditary spastic paraplegia 75 2024-05-06 criteria provided, single submitter clinical testing

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