Hi everyone,

I am new working with genetic data and I am starting with PLINK.

I have used the next command to identified all variants in one gene:

./plink2 --vcf chr19.dose.vcf.gz --from-bp position--to-bp position--chr 19 \
         --make-bed --out Variants_X_gene

And it has worked, but now, I have a list of all variants located in this gene in the .bim file, but I would like to identified the carriers of each variant.

How can I do that?

Thanks!!