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 |
not provided |
total |
|
61
|
102
|
214
|
39
|
15
|
5
|
394
|
Gene and significance breakdown #
Total genes and gene combinations: 2
| Gene or gene combination |
pathogenic |
likely pathogenic |
uncertain significance |
likely benign |
benign |
not provided |
total |
|
FANCG
|
61
|
102
|
213
|
39
|
15
|
5
|
393
|
|
intergenic
|
0 |
0 |
1
|
0 |
0 |
0 |
1
|
Submitter and significance breakdown #
| Submitter |
pathogenic |
likely pathogenic |
uncertain significance |
likely benign |
benign |
not provided |
total |
|
Natera, Inc.
|
18
|
36
|
91
|
12
|
7
|
0 |
164
|
|
Fulgent Genetics, Fulgent Genetics
|
12
|
17
|
104
|
17
|
0 |
0 |
150
|
|
Baylor Genetics
|
31
|
57
|
7
|
0 |
0 |
0 |
95
|
|
Illumina Laboratory Services, Illumina
|
0 |
0 |
38
|
6
|
7
|
0 |
51
|
|
Leiden Open Variation Database
|
41
|
1
|
7
|
0 |
0 |
0 |
49
|
|
St. Jude Molecular Pathology, St. Jude Children's Research Hospital
|
1
|
4
|
13
|
0 |
0 |
0 |
18
|
|
Genome-Nilou Lab
|
0 |
2
|
3
|
4
|
4
|
0 |
13
|
|
Revvity Omics, Revvity
|
5
|
3
|
5
|
0 |
0 |
0 |
13
|
|
KCCC/NGS Laboratory, Kuwait Cancer Control Center
|
1
|
0 |
0 |
1
|
7
|
0 |
9
|
|
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories
|
0 |
0 |
0 |
4
|
4
|
0 |
8
|
|
OMIM
|
8
|
0 |
0 |
0 |
0 |
0 |
8
|
|
Department of Pathology and Laboratory Medicine, Sinai Health System
|
1
|
1
|
2
|
0 |
0 |
0 |
4
|
|
GeneReviews
|
0 |
0 |
0 |
0 |
0 |
4
|
4
|
|
Molecular Diagnostics Laboratory, M Health Fairview: University of Minnesota
|
4
|
0 |
0 |
0 |
0 |
0 |
4
|
|
Neuberg Centre For Genomic Medicine, NCGM
|
0 |
4
|
0 |
0 |
0 |
0 |
4
|
|
3billion
|
2
|
0 |
1
|
0 |
0 |
0 |
3
|
|
Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre
|
2
|
1
|
0 |
0 |
0 |
0 |
3
|
|
Human Genetics Section, Sidra Medicine
|
1
|
2
|
0 |
0 |
0 |
0 |
3
|
|
Department of Maternal-Fetal Biology, National Research Institute for Child Health and Development
|
2
|
0 |
0 |
0 |
0 |
0 |
2
|
|
Laboratorio de Genetica e Diagnostico Molecular, Hospital Israelita Albert Einstein
|
1
|
1
|
0 |
0 |
0 |
0 |
2
|
|
Biochemical Molecular Genetic Laboratory, King Abdulaziz Medical City
|
0 |
0 |
1
|
0 |
0 |
0 |
1
|
|
Daryl Scott Lab, Baylor College of Medicine
|
1
|
0 |
0 |
0 |
0 |
0 |
1
|
|
Genetics and Molecular Pathology, SA Pathology
|
0 |
0 |
1
|
0 |
0 |
0 |
1
|
|
GenomeConnect - Invitae Patient Insights Network
|
0 |
0 |
0 |
0 |
0 |
1
|
1
|
|
Genomic Research Center, Shahid Beheshti University of Medical Sciences
|
0 |
0 |
1
|
0 |
0 |
0 |
1
|
|
Institute of Human Genetics, University of Leipzig Medical Center
|
1
|
0 |
0 |
0 |
0 |
0 |
1
|
|
Juno Genomics, Hangzhou Juno Genomics, Inc
|
1
|
0 |
0 |
0 |
0 |
0 |
1
|
|
Lifecell International Pvt. Ltd
|
0 |
1
|
0 |
0 |
0 |
0 |
1
|
|
Molecular Genetics, Royal Melbourne Hospital
|
0 |
0 |
0 |
0 |
1
|
0 |
1
|
|
Suma Genomics
|
1
|
0 |
0 |
0 |
0 |
0 |
1
|
|
UOSD Laboratory of Genetics & Genomics of Rare Diseases, Istituto Giannina Gaslini
|
0 |
0 |
1
|
0 |
0 |
0 |
1
|
|
Victorian Clinical Genetics Services, Murdoch Childrens Research Institute
|
0 |
0 |
1
|
0 |
0 |
0 |
1
|
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diagnostic use or medical decision-making without review by a
genetics professional. Individuals should not change their
health behavior solely on the basis of information contained on
this website. The submitted information has not been verified.
If you have questions about the information contained on this
website, please see a health care professional.