If you uploaded a variant set on Nov 29, 2023, your submission might have been lost. A problem has been fixed. Please simply upload the original query file. Sorry for the inconvenience.

Multi SNV lookup

This form allows you to quickly access the score (and annotation) of multiple single nucleotide variants (SNV). If you are investigating longer ranges of CADD SNV scores, you might be interested in our UCSC Genome Browser Tracks for hg19/GRCh37 and hg38/GRCh38. Please note that copying and downloading of the annotation tables is not working in Internet Explorer.

CADD scores are freely available for all non-commercial applications. If you are planning on using them in a commercial application, please contact us.

Chromosome:
Start: End:
CADD model: