List of variants in gene ETFDH reported as likely benign by Mayo Clinic Laboratories, Mayo Clinic

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_004453.4(ETFDH):c.1533T>C (p.Asp511=)	rs77484245	0.00552
NM_004453.4(ETFDH):c.1590A>G (p.Glu530=)	rs143015234	0.00114
NM_004453.4(ETFDH):c.1812G>A (p.Val604=)	rs17843967	0.00103
NM_004453.4(ETFDH):c.832-10T>G	rs200911913	0.00076

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