List of variants in gene combination LOC130056709, NIPA1 reported as uncertain significance for Hereditary spastic paraplegia

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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_144599.5(NIPA1):c.11C>T (p.Ala4Val)	rs1158637890
NM_144599.5(NIPA1):c.24GGC[10] (p.Ala15_Ala16dup)	rs531550505
NM_144599.5(NIPA1):c.24GGC[11] (p.Ala14_Ala16dup)	rs531550505

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