List of variants in gene ELOVL5 reported as not provided for Spinocerebellar ataxia type 38

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_021814.5(ELOVL5):c.246+3891C>T	rs150583340	0.00704
NM_021814.5(ELOVL5):c.214C>G (p.Leu72Val)	rs587777671
NM_021814.5(ELOVL5):c.689G>T (p.Gly230Val)	rs587777670

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