ClinVar Miner

Variants studied for argininosuccinic aciduria

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
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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 total
32 27 45 13 7 114

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 total
ASL 32 27 45 13 7 114

Submitter and significance breakdown #

Total submitters: 15
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign total
Counsyl 9 26 30 1 0 66
Invitae 9 2 7 5 7 30
Illumina Clinical Services Laboratory,Illumina 2 1 9 7 0 19
SNPedia 11 0 0 0 0 11
Integrated Genetics/Laboratory Corporation of America 7 0 0 0 0 7
OMIM 6 0 0 0 0 6
GeneReviews 3 0 0 0 0 3
Fulgent Genetics 3 0 0 0 0 3
Genetic Services Laboratory, University of Chicago 2 0 0 0 0 2
Genome Diagnostics Laboratory,University Medical Center Utrecht 2 0 0 0 0 2
Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine 0 1 0 0 0 1
Genomic Research Center,Shahid Beheshti University of Medical Sciences 1 0 0 0 0 1
Knight Diagnostic Laboratories,Oregon Health and Sciences University 1 0 0 0 0 1
SIB Swiss Institute of Bioinformatics 0 1 0 0 0 1
Department of Genetics,Sultan Qaboos University Hospital, Oman 1 0 0 0 0 1

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