regSNP-intron

regSNP-intron predicts the disease-causing probability of human intronic single nucleotide variants (iSNVs).

View a sample result page .

Enter tab-delimited variants, for example chr1 100 A G, or use the example input button.

Optional. Maximum size: 10,000 rows.
Optional.
Optional. If provided, the site will send a notification when processing finishes.