List of variants in gene ELOVL4 reported as uncertain significance by Institute of Human Genetics, Univ. Regensburg, Univ. Regensburg

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_022726.4(ELOVL4):c.800T>C (p.Ile267Thr)	rs148594713	0.00636
NM_022726.4(ELOVL4):c.53C>T (p.Ala18Val)
NM_022726.4(ELOVL4):c.596A>G (p.Tyr199Cys)
NM_022726.4(ELOVL4):c.818C>A (p.Pro273His)

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