ClinVar Miner

List of variants in gene ETFB reported as likely benign for acyl-CoA dehydrogenase deficiency

Included ClinVar conditions (6):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 8
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HGVS dbSNP
NM_001985.3(ETFB):c.253C>A (p.Arg85=) rs187424345
NM_001985.3(ETFB):c.292C>T (p.Arg98Cys) rs147353781
NM_001985.3(ETFB):c.452C>T (p.Ser151Phe) rs74735908
NM_001985.3(ETFB):c.521G>A (p.Arg174His) rs141917423
NM_001985.3(ETFB):c.565G>A (p.Glu189Lys) rs376065198
NM_001985.3(ETFB):c.577G>A (p.Ala193Thr) rs200186078
NM_001985.3(ETFB):c.58-212A>C rs143144671
NM_001985.3(ETFB):c.58-318_58-313dup rs61361626

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