ClinVar Miner

Submissions for variant NM_015346.4(ZFYVE26):c.2222del (p.Lys741fs) (rs1555399288)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Molecular Genetics Laboratory,BC Children's and BC Women's Hospitals RCV000578441 SCV000680102 likely pathogenic Hereditary spastic paraplegia 15 2016-10-31 no assertion criteria provided clinical testing

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