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v2025.1
About
FAVORannotator
Forums
Team
Terms
Newsletter
Documentation
What's New
v2025.1
17-43125086-43125731
Chr 17
Genomic region (646 bp)
Chromosome: 17
Start position: 43,125,086
End position: 43,125,731
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
6
% of Total
0.0284
Benign:
6
0.0284
Likely Benign:
Count
12
% of Total
0.0569
Likely Benign:
12
0.0569
Uncertain Significance:
Count
10
% of Total
0.0474
Uncertain Significance:
10
0.0474
Conflicting Interpretations:
Count
0
% of Total
0.0000
Conflicting Interpretations:
0
0.0000