uVariants at dna-utah.org - The Awesome Primer Design Tool - All Rights Reserved 2025

Welcome

SNP information can be difficult to consolidate. Streamline and improve your assay design with uVariants .

rs #

+/-bp

X

Once sequence is returned, hover over annotated nucleotides for more information:

(X/Y) SNP of Interest
[X/Y] Neighboring SNPs with Frequencies Reported
[X/Y] Neighboring SNPS with No Frequency Reported
X Nucleotide (as 3'end) has high frequency in genome
Y Nucleotide (as 3'end) has low frequency in genome

X Allele: