Retrieve functional, structural annotations and frequency statistics by entering a list of
gene variations (cDNA, protein, genomic descriptions). Each dataset entry corresponds to a
unique gene variation.
Retrieve functional, structural annotations and frequency statistics by entering various features of the variants. Each dataset entry corresponds to a
unique gene variation.
See a list of polymorphisms which are variants that have been observed in unaffected human
population at frequency > 0.001 in at least one of the following databases: 1000G, gnomAD,
or ESP6500.