ClinVar Miner

Variants studied for congenital sucrase-isomaltase deficiency

Included ClinVar conditions (1):
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 total
8 4 126 11 16 162

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 total
SI 8 4 126 11 16 162

Submitter and significance breakdown #

Total submitters: 9
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign total
Illumina Clinical Services Laboratory,Illumina 3 0 124 11 16 154
OMIM 8 0 0 0 0 8
Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine 0 3 0 0 0 3
Baylor Genetics 0 1 1 0 0 2
Mendelics 1 0 1 0 0 2
Division of Human Genetics,Children's Hospital of Philadelphia 2 0 0 0 0 2
Rady Children's Institute for Genomic Medicine, Rady Children's Hospital San Diego 0 2 0 0 0 2
Genomic Research Center, Shahid Beheshti University of Medical Sciences 0 0 1 0 0 1
New York Genome Center 0 0 1 0 0 1

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