Single Nucleotide Polymorphisms
GPTKB entity
Statements (52)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:Genetic_variation
|
| gptkbp:abbreviation |
gptkb:SNPs
|
| gptkbp:affects |
gptkb:protein
Gene expression Gene function |
| gptkbp:associatedWith |
Infectious diseases
Ancestry Cardiovascular diseases Genetic disorders Autoimmune diseases Cancer risk Disease susceptibility Drug response Metabolic diseases Neurological diseases Trait variation |
| gptkbp:averageFrequency |
1 in every 300 nucleotides
|
| gptkbp:canBe |
Forensic identification
Paternity testing Plant breeding Evolutionary studies Animal breeding Exonic Genetic diversity assessment Genetic mapping Intergenic Intronic Linkage analysis Marker-assisted selection Non-synonymous Population structure analysis Synonymous |
| gptkbp:cataloguedIn |
gptkb:dbSNP
|
| gptkbp:defines |
Variation at a single position in a DNA sequence among individuals
|
| gptkbp:detects |
PCR
DNA sequencing Microarray analysis |
| gptkbp:firstDescribed |
1990s
|
| gptkbp:foundIn |
gptkb:gene
|
| gptkbp:frequency |
Common in human genome
|
| gptkbp:studiedBy |
Medical researchers
Geneticists Bioinformaticians |
| gptkbp:usedIn |
Personalized medicine
Disease risk assessment Genetic association studies Genome-wide association studies Pharmacogenomics Population genetics |
| gptkbp:bfsParent |
gptkb:SNPs
|
| gptkbp:bfsLayer |
7
|
| https://www.w3.org/2000/01/rdf-schema#label |
Single Nucleotide Polymorphisms
|