List of variants in gene CYP2U1 reported as benign for hereditary spastic paraplegia

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_183075.3(CYP2U1):c.1127-17T>C	rs6856745	0.63755
NM_183075.3(CYP2U1):c.*31A>G	rs79009744	0.02566
NM_183075.3(CYP2U1):c.*132G>T	rs80203932

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