ClinVar Miner

List of variants in gene SPG11 reported by Consultorio y Laboratorio de Neurogenética, Hospital JM Ramos Mejia

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_025137.4(SPG11):c.6205+1G>A	rs753650233	0.00001
NM_025137.4(SPG11):c.6832_6833del (p.Ser2278fs)	rs312262784

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