List of variants in gene ELOVL4 reported as uncertain significance for syndromic dyslipidemia

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_022726.4(ELOVL4):c.351T>A (p.Asn117Lys)	rs148018494	0.00031
NM_022726.4(ELOVL4):c.226C>T (p.Arg76Cys)	rs371760799

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