I am wondering how you find out which are the risk alleles, or mutations that potentially cause disease.
For instance I found out which genes to look for for Ehlers Danlos--in my raw data there are gobs of
homozygous results, but I don't know how to tell which versions are the normal or the risk alleles.
Mutations in the following can cause Ehlers–Danlos syndrome:
Can someone help? On a steep learning curve with the genetic stuff.
I currently have no less that 15 ribs out of place (super painful), so I'm thinking EDS right about now and would like to know more.
For instance I found out which genes to look for for Ehlers Danlos--in my raw data there are gobs of
homozygous results, but I don't know how to tell which versions are the normal or the risk alleles.
Mutations in the following can cause Ehlers–Danlos syndrome:
Can someone help? On a steep learning curve with the genetic stuff.
I currently have no less that 15 ribs out of place (super painful), so I'm thinking EDS right about now and would like to know more.