Hi Priyabrata,
Not exactly. This is something that I've already done as you can see on the image above. Each polymorphism were coded as 0/1/2 based on their genotype combination (e.g AA = 0, AG = 1, GG = 2).
I have determined the phase (with PHASE program) of these 13 polymorphism, generating 17 unique haplotypes distributed across my case-control study...Now I want to do a regression analysis to see if one of those (or more) 17 haplotypes might be associated with my disease (taking into consideration on the regression model, the two PCs in order to control for population stratification). The two PCs can be seen on the last two columns of the picture above...
