Gene based analysis

People are often interested in gene X. Do we have any patients with interesting variants?

At the moment we can do it using the all variants node, but then you end up having to go through the ~200 variants by hand - most of the time they're in control samples or samples with totally unrelated phenotypes etc.

So basically when he says that he means can you look at affecteds in the certain cohorts, not parents or marry-ins.