ClinVar Miner

Submissions for variant NM_004722.4(AP4M1):c.147+10G>A

dbSNP: rs1584505112
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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 RCV000977978 SCV001125902 likely benign Hereditary spastic paraplegia 50 2019-12-31 criteria provided, single submitter clinical testing

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