ClinVar Miner

Variants studied for diabetes mellitus, permanent neonatal 3

Included ClinVar conditions (4):
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
51 68 219 41 19 396

Gene and significance breakdown #

Total genes and gene combinations: 3
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Gene or gene combination pathogenic likely pathogenic uncertain significance likely benign benign total
ABCC8 49 68 209 35 16 375
ABCC8, LOC110121471 2 0 10 6 2 20
ABCC8, KCNJ11 0 0 0 0 1 1

Submitter and significance breakdown #

Total submitters: 10
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign total
Fulgent Genetics, Fulgent Genetics 42 66 216 38 3 365
Pars Genome Lab 0 0 1 3 16 20
OMIM 9 0 0 0 0 9
New York Genome Center 1 0 3 0 0 4
Genome-Nilou Lab 0 0 1 0 1 2
MGZ Medical Genetics Center 0 0 1 0 0 1
Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center 1 0 0 0 0 1
Juno Genomics, Hangzhou Juno Genomics, Inc 0 0 1 0 0 1
Molecular Genetics and NGS Laboratory, Hospital Fundacion Valle Del Lili 0 1 0 0 0 1
MVZ Medizinische Genetik Mainz 0 1 0 0 0 1

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