About
FAVORannotator
Forums
Team
Terms
Newsletter
Documentation
What's New
v2025.1
About
FAVORannotator
Forums
Team
Terms
Newsletter
Documentation
What's New
v2025.1
17-43125302-43125731
Chr 17
Genomic region (430 bp)
Chromosome: 17
Start position: 43,125,302
End position: 43,125,731
SNV Summary
InDel Summary
Single Cell/Tissue
Full Tables
Genome Browser
Clinvar Clinical Significance
© 2026 Harvard T.H Chan School of Public Health, Inc. All rights reserved.
Chat with FAVOR-GPT
Visualization
Chart
Table View
Table
Annotation
Count
% of Total
Drug Response:
Count
0
% of Total
0.0000
Drug Response:
0
0.0000
Pathogenic:
Count
0
% of Total
0.0000
Pathogenic:
0
0.0000
Likely Pathogenic:
Count
0
% of Total
0.0000
Likely Pathogenic:
0
0.0000
Benign:
Count
3
% of Total
0.0205
Benign:
3
0.0205
Likely Benign:
Count
1
% of Total
0.0068
Likely Benign:
1
0.0068
Uncertain Significance:
Count
8
% of Total
0.0548
Uncertain Significance:
8
0.0548
Conflicting Interpretations:
Count
0
% of Total
0.0000
Conflicting Interpretations:
0
0.0000