URL: http://www.ncbi.nlm.nih.gov/SNP/
Proper Citation: dbSNP (RRID:SCR_002338)
Description: Database as central repository for both single base nucleotide substitutions and short deletion and insertion polymorphisms. Distinguishes report of how to assay SNP from use of that SNP with individuals and populations. This separation simplifies some issues of data representation. However, these initial reports describing how to assay SNP will often be accompanied by SNP experiments measuring allele occurrence in individuals and populations. Community can contribute to this resource.
Abbreviations: dbSNP
Synonyms: dbSNP: Database for Short Genetic Variations, Entrez SNP - Single Nucleotide Polymorphism, SNV Database, NCBI SNV Database, NCBI Short Genetic Variations Database, NCBI Short Genetic Variations, NCBI Single Nucleotide Polymorphism, Entrez SNP, dbSNP, NCBI Short Genetic Variations (SNV) database
Resource Type: data or information resource, service resource, data repository, database, storage service resource
Defining Citation: PMID:21154707
Keywords: insertion, polymorphism, short, deletion, single, nucleotide, genetic, variation, genomics, genotype, disease, allele, microsatellite, marker, multinucleotide, heterozygous, sequence, gold standard, bio.tools
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NIDDK - National Institute of Diabetes and Digestive and Kidney Diseases |
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