Check this box to combine rare variants within a gene (or other unit, as defined by the
Annotation Analysis Group Variable
) and specify coding as
1
if any rare
alleles
are present in any
SNP
belonging to the gene or group, and
0
otherwise.
If
not
checked, rare variants are coded individually according to a dominant model, that is,
1
if any rare alleles are present in the SNP, and
0
otherwise.
