ClinVar Miner

Submissions for variant NM_015346.4(ZFYVE26):c.886+1G>C

dbSNP: rs752618765
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Baylor Genetics RCV001328901 SCV001520140 pathogenic Hereditary spastic paraplegia 15 2019-02-02 criteria provided, single submitter clinical testing This variant was determined to be pathogenic according to ACMG Guidelines, 2015 [PMID:25741868].

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