ClinVar Miner

Submissions for variant NM_015161.3(ARL6IP1):c.37-20T>G

dbSNP: rs1219663998
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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 RCV002863684 SCV003232517 likely benign Hereditary spastic paraplegia 61 2022-09-05 criteria provided, single submitter clinical testing

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