C1849128[trait identifier] AND "Mayo Clinic Laboratories, Mayo Clinic" - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 188338	NM_015346.4(ZFYVE26):c.7055C>T (p.Thr2352Ile)	ZFYVE26 (T2352I)	Single nucleotide variant (missense variant)	Spastic paraplegia +4 more	GConflicting classifications of pathogenicity
Select item 1027979	NM_015346.4(ZFYVE26):c.6649C>G (p.Leu2217Val)	ZFYVE26 (L2217V)	Single nucleotide variant (missense variant)	Spastic paraplegia +2 more	GUncertain significance
Select item 1163951	NM_015346.4(ZFYVE26):c.5834G>A (p.Arg1945Gln)	ZFYVE26 (R1945Q)	Single nucleotide variant (missense variant)	Spastic paraplegia +3 more	GUncertain significance
Select item 241050	NM_015346.4(ZFYVE26):c.5401G>A (p.Ala1801Thr)	ZFYVE26 (A1801T)	Single nucleotide variant (missense variant)	Spastic paraplegia +2 more	GUncertain significance
Select item 649757	NM_015346.4(ZFYVE26):c.4452G>C (p.Arg1484Ser)	ZFYVE26 (R1484S)	Single nucleotide variant (missense variant)	Spastic paraplegia +4 more	GUncertain significance
Select item 313923	NM_015346.4(ZFYVE26):c.763C>T (p.Arg255Trp)	ZFYVE26 (R255W)	Single nucleotide variant (missense variant)	Hereditary spastic paraplegia 15 +3 more	GUncertain significance

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