Identification and mapping of single nucleotide polymorphisms in the human genome

Document Number: H0002191

Abstract:

The invention relates to the role of genes in human diseases. More particularly, the invention relates to compositions and methods for identifying genes that are involved in human disease conditions. The invention provides identification and mapping of a very large number of SNPs throughout the entire human genome. This contribution allows scientists to isolate and identify genes that are relevant to the prevention, causation, or treatment of human disease conditions.

Application Number: 09925065

Primary Class: 435 6

Sub-Classes: 536 2433, 536 243, 536 231

Inventors: David G. Wang, Lake Zurich, IL, US

Assignee: SNP Consortium, Chicago, US

Examiners: M. Clement (primary)

Filing Date: 2001-08-08

Publication Date: 2007-06-05

PDF: H0002191

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