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 |
5
|
12
|
6
|
1
|
0 |
21
|
Gene and significance breakdown #
Total genes and gene combinations: 1
Gene or gene combination |
pathogenic |
likely pathogenic |
uncertain significance |
likely benign |
total |
CCDC8
|
5
|
12
|
6
|
1
|
21
|
Submitter and significance breakdown #
Submitter |
pathogenic |
likely pathogenic |
uncertain significance |
likely benign |
total |
Women's Health and Genetics/Laboratory Corporation of America, LabCorp
|
1
|
5
|
0 |
0 |
6
|
Fulgent Genetics, Fulgent Genetics
|
0 |
3
|
1
|
1
|
5
|
OMIM
|
3
|
0 |
0 |
0 |
3
|
Baylor Genetics
|
0 |
1
|
2
|
0 |
3
|
Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre
|
0 |
2
|
1
|
0 |
3
|
Centre for Mendelian Genomics, University Medical Centre Ljubljana
|
0 |
2
|
0 |
0 |
2
|
Revvity Omics, Revvity
|
0 |
0 |
1
|
0 |
1
|
Biochemical Molecular Genetic Laboratory, King Abdulaziz Medical City
|
0 |
1
|
0 |
0 |
1
|
Molecular Genetics Laboratory, Motol Hospital
|
0 |
1
|
0 |
0 |
1
|
Division of Medical Genetics, Department of Pediatrics, All India Institute of Medical Sciences, New Delhi
|
0 |
0 |
1
|
0 |
1
|
Dr.Nikuei Genetic Center
|
1
|
0 |
0 |
0 |
1
|
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