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v2025.1
About
FAVORannotator
Forums
Team
Terms
Newsletter
Documentation
What's New
v2025.1
17-43125334-43125736
Chr 17
Genomic region (403 bp)
Chromosome: 17
Start position: 43,125,334
End position: 43,125,736
SNV Summary
InDel Summary
Single Cell/Tissue
Full Tables
Genome Browser
Clinvar Clinical Significance
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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
0.0221
Benign:
3
0.0221
Likely Benign:
Count
1
% of Total
0.0074
Likely Benign:
1
0.0074
Uncertain Significance:
Count
4
% of Total
0.0294
Uncertain Significance:
4
0.0294
Conflicting Interpretations:
Count
0
% of Total
0.0000
Conflicting Interpretations:
0
0.0000