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 |
11
|
13
|
1
|
0 |
0 |
24
|
Gene and significance breakdown #
Total genes and gene combinations: 1
Gene or gene combination |
pathogenic |
likely pathogenic |
uncertain significance |
total |
GHRHR
|
11
|
13
|
1
|
24
|
Submitter and significance breakdown #
Submitter |
pathogenic |
likely pathogenic |
uncertain significance |
total |
OMIM
|
7
|
0 |
0 |
7
|
Women's Health and Genetics/Laboratory Corporation of America, LabCorp
|
4
|
2
|
0 |
6
|
Fulgent Genetics, Fulgent Genetics
|
2
|
4
|
0 |
6
|
Revvity Omics, Revvity
|
2
|
1
|
1
|
4
|
Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre
|
0 |
2
|
0 |
2
|
Beijing Key Laboratory for Genetic Research of Skeletal Deformity, Peking Union Medical College Hospital
|
0 |
2
|
0 |
2
|
Neuberg Centre For Genomic Medicine, NCGM
|
1
|
1
|
0 |
2
|
Institute of Human Genetics Munich, Klinikum Rechts Der Isar, TU München
|
1
|
0 |
0 |
1
|
Genetics and Genomic Medicine Centre, NeuroGen Healthcare, NeuroGen Healthcare
|
1
|
0 |
0 |
1
|
Istanbul Faculty of Medicine, Istanbul University
|
1
|
0 |
0 |
1
|
3billion
|
1
|
0 |
0 |
1
|
Center of Human Genetics, Hôpital Erasme
|
0 |
1
|
0 |
1
|
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