Hi all,
I want to know how I can tell if a variant I got is a common SNP or not using UCSC genome browser.
For example, if I got 1:115258683-A>A/C on GRCh37, how can I check if this is a common SNP or rare SNP?
I found that there is "dbSNP 155" in "Variation" in the genome browser, but not sure how I can set it up and check.
Thank you!