ClinVar Miner

Submissions for variant NM_031448.6(C19orf12):c.120C>T (p.Phe40=)

dbSNP: rs1972486377
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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 RCV003743380 SCV004483636 likely benign Hereditary spastic paraplegia 43 2024-10-25 criteria provided, single submitter clinical testing

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