USH2220HExpiredUtilityA1

Identification and mapping of single nucleotide polymorphisms in the human genome

83
Assignee: SNP CONSORTIUMPriority: Aug 10, 2001Filed: Nov 21, 2002Granted: Jul 1, 2008
Est. expiryAug 10, 2021(expired)· nominal 20-yr term from priority
Inventors:WANG DAVID G
C12Q 2600/156C12Q 1/6883
83
PatentIndex Score
18
Cited by
0
References
1
Claims

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.

Claims

exact text as granted — not AI-modified
1. A SNP probe consisting of an oligonucleotide that is complementary to a SNP nucleic acid selected from the SNP nucleic acids shown in SEQ ID NOs.:1-1,226,818.

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