ClinVar Miner

List of variants in gene SPG11 reported as likely pathogenic by Department of Hematologic Diagnostics and Genetics, Jagiellonian University Hospital in Krakow

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 1

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HGVS	dbSNP	gnomAD frequency
NM_025137.4(SPG11):c.6404del (p.Ile2135fs)	rs2140923130

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