{{Rsnum
|rsid = 3177751
|geno1 = (C;C)
|geno2 = (C;T)
|geno3 = (T;T)
|Status = Merged
|Merged = 1130426
|Gene = ETFB
|Orientation=minus
|ReferenceAllele=C
|MissenseAllele=T
|Chromosome=19
|position=51347036
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ETFB
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 18.6 | 45.1 | 36.3
| HCB | 56.2 | 35.0 | 8.8
| JPT | 55.8 | 37.2 | 7.1
| YRI | 20.4 | 57.8 | 21.8
| ASW | 29.8 | 54.4 | 15.8
| CHB | 56.2 | 35.0 | 8.8
| CHD | 52.3 | 38.5 | 9.2
| GIH | 37.6 | 48.5 | 13.9
| LWK | 20.9 | 47.3 | 31.8
| MEX | 39.7 | 43.1 | 17.2
| MKK | 15.4 | 58.3 | 26.3
| TSI | 18.6 | 52.9 | 28.4
| HapMapRevision=28
}}

{{Venter SNP
|rsid=3177751
|allele=A
|frequency=
|uid=1103691166320
|type=heterozygous_SNP
|hugo=ETFB
|ensembl gene=ENSG00000105379
|ensembl transcript=ENST00000309244
|sift=AFFECT FUNCTION
|disease=Defects in ETFB are the cause of glutaric aciduria type IIB (GAIIB) (MIM:231680); also known as glutaricaciduria IIB. GAIIB results in the excretion not only of glutaric acid but also of lactic, ethylmalonic, butyric, isobutyric, 2-methyl-butyric, and isovaleric acids. It is seen in its most severe form in infancy, with polycystic and dysplastic kidneys, hypoketotic acidosis and hypoglycemia that can lead to death. The milder form can be characterized by recurrent episodes of lasting lethargy or slowly progressive myopathy.
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}