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 |
72
|
160
|
115
|
26
|
4
|
365
|
Gene and significance breakdown #
Total genes and gene combinations: 45
Submitter and significance breakdown #
Submitter |
pathogenic |
likely pathogenic |
uncertain significance |
likely benign |
benign |
total |
Baylor Genetics
|
46
|
33
|
73
|
0 |
0 |
152
|
Database of Curated Mutations (DoCM)
|
0 |
100
|
0 |
0 |
0 |
100
|
Fulgent Genetics, Fulgent Genetics
|
14
|
5
|
20
|
25
|
4
|
68
|
Genome Sciences Centre, British Columbia Cancer Agency
|
3
|
6
|
21
|
0 |
0 |
30
|
Key Laboratory of Carcinogenesis and Cancer Invasion, Central South University
|
0 |
19
|
0 |
0 |
0 |
19
|
OMIM
|
7
|
0 |
0 |
0 |
0 |
7
|
Institute of Human Genetics Munich, Klinikum Rechts Der Isar, TU München
|
7
|
0 |
0 |
0 |
0 |
7
|
Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center
|
3
|
1
|
1
|
1
|
0 |
6
|
Ute Scholl Laboratory, Heinrich Heine University Duesseldorf
|
5
|
0 |
0 |
0 |
0 |
5
|
Donald Williams Parsons Laboratory, Baylor College of Medicine
|
0 |
1
|
0 |
0 |
0 |
1
|
Centre for Mendelian Genomics, University Medical Centre Ljubljana
|
0 |
0 |
1
|
0 |
0 |
1
|
Diagnostics Services (NGS), CSIR - Centre For Cellular And Molecular Biology
|
0 |
1
|
0 |
0 |
0 |
1
|
Genome-Nilou Lab
|
1
|
0 |
0 |
0 |
0 |
1
|
Suma Genomics
|
1
|
0 |
0 |
0 |
0 |
1
|
Neuberg Centre For Genomic Medicine, NCGM
|
0 |
0 |
1
|
0 |
0 |
1
|
MVZ Medizinische Genetik Mainz
|
0 |
0 |
1
|
0 |
0 |
1
|
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