How do you interpret Human sequence variants from exome/clinical exome or panel sequencing?

9 votes
Public domain
 
33% / 3 votes
Commercial (IPA, DNAstar, SAP and others)
 
33% / 3 votes
Combinations
 
33% / 3 votes
Homemade database
 
0% / 0 votes
Why Me Worry?
 
0% / 0 votes


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