I would like to test the association between different SNPs and a marker, however, by using
PLINK command:
./plink2 --bfile NewFileWithSNPsInABCG5GRCh37new --pheno AllPhenotypes.txt --pheno-name CAMPE --covar Cova.txt --covar-name S1,S2,S4,S10,S17 --linear --out name_ABCG5_AssoCampe_S1_S2_S4,S10,S17
an additive model was built. However, I would like to know if – for example – there is a difference at all between AA, AB and BB. I am not specifically looking for additive / dominant / recessive models. But I would like to compare the three genotype. Is a command for that in PLINK?
Thank you in advance,
Fatma