ClinVar Miner

Submissions for variant NM_015346.4(ZFYVE26):c.7257del (p.Lys2418_Tyr2419insTer)

dbSNP: rs771393692
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000674314 SCV000799630 likely pathogenic Hereditary spastic paraplegia 15 2018-05-01 criteria provided, single submitter clinical testing

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