ClinVar Miner

Submissions for variant NM_025137.4(SPG11):c.359del (p.Asn119_Leu120insTer)

dbSNP: rs312262712
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneReviews RCV000034208 SCV000058146 not provided Hereditary spastic paraplegia 11 no assertion provided literature only

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