ClinVar Miner

Submissions for variant NM_014846.4(WASHC5):c.2087G>C (p.Gly696Ala)

dbSNP: rs397515564
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneReviews RCV000055943 SCV000086968 not provided Hereditary spastic paraplegia 8 no assertion provided literature only
OMIM RCV000055943 SCV000109620 pathogenic Hereditary spastic paraplegia 8 2013-07-01 no assertion criteria provided literature only

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