ClinVar Miner

Variants studied for Deficiency of butyryl-CoA dehydrogenase

Coded as:
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:

If a variant has more than one submission, it may be counted in more than one significance column. If this is the case, the total number of variants will be less than the sum of the other cells.

pathogenic likely pathogenic uncertain significance likely benign benign not provided total
16 37 114 5 14 3 162

Gene and significance breakdown #

Total genes and gene combinations: 1
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Gene or gene combination pathogenic likely pathogenic uncertain significance likely benign benign not provided total
ACADS 16 37 114 5 14 3 162

Submitter and significance breakdown #

Total submitters: 16
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign not provided total
Counsyl 2 33 36 0 0 0 71
Illumina Clinical Services Laboratory,Illumina 3 2 38 2 14 0 59
Invitae 3 4 45 2 3 0 57
OMIM 16 0 0 0 0 0 16
Fulgent Genetics,Fulgent Genetics 3 1 0 0 0 0 4
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories 0 0 0 0 3 0 3
GeneReviews 1 2 0 0 0 0 3
Genomic Research Center, Shahid Beheshti University of Medical Sciences 0 2 1 0 0 0 3
GenomeConnect, ClinGen 0 0 0 0 0 3 3
Mendelics 0 0 1 1 0 0 2
Reproductive Health Research and Development,BGI Genomics 2 0 0 0 0 0 2
Laboratory for Molecular Medicine, Partners HealthCare Personalized Medicine 1 0 0 0 0 0 1
Knight Diagnostic Laboratories, Oregon Health and Sciences University 1 0 0 0 0 0 1
Biochemical Molecular Genetic Laboratory,King Abdulaziz Medical City 0 1 0 0 0 0 1
Molecular Diagnostics Laboratory, M Health: University of Minnesota 0 1 0 0 0 0 1
Myriad Women's Health, Inc. 1 0 0 0 0 0 1

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