Hi,
I've seen that some people annotate their sequencing data with dbSNP135_common (contains variants with allele frequency >1%) and dbSNP135_full (contains all types of variants including disease variants also). I'm using annovar for my data, is there any way to do this in annovar? Where can I download these two versions?
Thanks,
I've seen that some people annotate their sequencing data with dbSNP135_common (contains variants with allele frequency >1%) and dbSNP135_full (contains all types of variants including disease variants also). I'm using annovar for my data, is there any way to do this in annovar? Where can I download these two versions?
Thanks,
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