ClinVar Miner

Submissions for variant NM_031448.6(C19orf12):c.165G>T (p.Gly55=)

dbSNP: rs201194487
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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 RCV002235479 SCV002510889 likely benign Hereditary spastic paraplegia 43 2023-06-17 criteria provided, single submitter clinical testing

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