ClinVar Miner

Submissions for variant NM_001160148.2(DDHD1):c.1012+645C>T

dbSNP: rs1595179182
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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 RCV001472453 SCV001676586 likely benign Hereditary spastic paraplegia 28 2022-08-28 criteria provided, single submitter clinical testing

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