Thanks for pointing that out I checked and they werent.
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I have a list of dbSNP rs ids and I would like to get scores for the 16 or 17 annotation tools as used by annovar. When I run annovar on these rsids. I get a lot of missing values rows (around 16k out of a list of 20k). Is there any way I can get these annotation scores with minimum fuss.
Sift and PolyPhen are only for missense variants that alter the amino acid sequence. Are all your variants missense?
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