OK, maybe some of you can help me interpret my results and decide what to do with them. Here's how my file begins:
# This data file generated by DNA Diagnostic Center™'s Dream Array at: Mon Nov 06 10:19:56 2017
#
# Below is a text version of your data. Fields are TAB-separated
# Each line corresponds to a single SNP. For each SNP, we provide its identifier
# (an rsid or an internal id), its location on the reference human genome, and the
# genotype call tied to the plus strand on the human reference sequence.
# We are using reference human assembly build 37 (also known as Annotation Release 104).
#
#
#
#
#
#rsid chromosome position genotype
rs1000440 9 101258881 TT
rs10007601 4 164934874 AG
rs10056215 5 163542505 TG
rs10075407 5 2993645 AG
rs10150378 14 44000834 TT
rs10196277 2 149188375 TG
rs1021996 12 51789617 CC
After this, there are literally almost 800,000 similar lines of code. How do I compare this to the other data people are posting?