Variant view

The variant view has the following URL: http://r2.finngen.fi/variant/CHR-POS-ALT-REF, e.g. http://r2.finngen.fi/variant/13-80757865-T-TA

• CHR: chromosome on hg38 (1-22, X or 23)

• POS: position on hg38

• REF: reference allele

• ALT: alternative allele

Variant view: displaying on the x-axis all phenotypes and phenotype categories and on the y-axis the p-values.