List of variants in gene ETFA reported as uncertain significance by CeGaT Center for Human Genetics Tuebingen

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_000126.4(ETFA):c.20C>T (p.Pro7Leu)	rs557160401	0.00027
NM_000126.4(ETFA):c.187G>T (p.Val63Leu)
NM_000126.4(ETFA):c.37G>A (p.Ala13Thr)	rs769838321

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