I am an IT guy developing a database for genotype data of samples and I am confused when I look up a snp in NCBI, the genes listed for that SNP sometimes have multiple consequences (intron, missense, upstream, etc.) but on the data that I received only one of those consequences is listed.
Question: Why do genes have multiple consequences for the same SNP?
23 months ago by
first • 30
first • 30 wrote:
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