ClinVar Miner

Submissions for variant NM_025137.4(SPG11):c.2198T>G (p.Leu733Ter)

dbSNP: rs312262739
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneReviews RCV000034188 SCV000058126 not provided Hereditary spastic paraplegia 11 no assertion provided literature only
OMIM RCV000034188 SCV000249583 pathogenic Hereditary spastic paraplegia 11 2010-02-01 no assertion criteria provided literature only
OMIM RCV000192703 SCV000249584 pathogenic Amyotrophic lateral sclerosis type 5 2010-02-01 no assertion criteria provided literature only

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