Large Numbers of Genetic Variants Considered to be Pathogenic are Common in Asymptomatic Individuals
It is now affordable to order clinically interpreted whole-genome sequence reports from clinical laboratories. One major component of these reports is derived from the knowledge base of previously identified pathogenic variants, including research articles, locus-specific, and other databases. While...
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Format: | Article |
Language: | en_US |
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Wiley Blackwell
2014
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Online Access: | http://hdl.handle.net/1721.1/89413 |