List of variants in gene combination EIF3J, SPG11 reported as uncertain significance for Spastic Paraplegia, Recessive

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_003758.4(EIF3J):c.1574_1578dup	rs886051173	0.00004
NM_003758.4(EIF3J):c.1601_1604dup	rs886051174	0.00003
NM_003758.4(EIF3J):c.*1652G>A	rs886051175

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