ClinVar Miner

Variants studied for autosomal systemic lupus erythematosus type 16

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
2 1 27 12 0 42

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 total
DNASE1L3 2 1 27 12 42

Submitter and significance breakdown #

Total submitters: 8
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Submitter pathogenic likely pathogenic uncertain significance likely benign total
Fulgent Genetics, Fulgent Genetics 0 0 24 12 36
Undiagnosed Diseases Network, NIH 1 0 1 0 2
3billion 0 0 2 0 2
OMIM 1 0 0 0 1
Kasturba Medical College, Manipal, Kasturba Medical College, Manipal, Manipal Academy of Higher Education, Manipal, India 1 0 0 0 1
Rady Children's Institute for Genomic Medicine, Rady Children's Hospital San Diego 1 0 0 0 1
Genomics Facility, Ludwig-Maximilians-Universität München 0 1 0 0 1
Suma Genomics 1 0 0 0 1

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