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rs6295, also called C(-1019)G, is a gene variation—a single nucleotide polymorphism (SNP)—in the HTR1A gene. It is one of the most investigated SNPs of its gene. The C-allele is the most prevalent with 0.675 against the G-allele with 0.325 among Caucasian.
The analysis highlights Regions, Personality and Disorders as prominent areas in the source structure around Rs6295.
Source areas are shown by the number of related topics found in each part of the analysis. Use smaller areas too: they can reveal specialized angles and content gaps.
Smaller areas are not necessarily less important. They contain fewer connections in this analysis and can be useful for finding specialized angles or coverage gaps.
High-confidence facts extracted from structured source data. Use them as anchors for further research.
Browse the complete topic structure, not only the most central items. Less prominent entities and concepts can reveal missing angles, specialized context and useful research gaps. Each item opens a new analysis centered on that subject.
Deeper signals for content research, entity SEO and topical coverage. The plain-language headings explain what each technical view is useful for.
The extracted context around Rs6295 shows recurring relationship patterns in the source. For example, Rs6295 → 5 Another extracted example is Rs6295 → 6295. Use these groups to spot repeated connection types before inspecting the individual relationships.
Use these terms to understand the vocabulary surrounding the topic, not as a checklist for keyword stuffing.
gene g-allele one study snp htr1a snps association studies polymorphism investigated disorders personality -1019 human found disorder also among caucasian
TTTA extracted 8 structured relationships around Rs6295. Examples in this analysis include Rs6295 → Chromosome → 5 and Rs6295 → dbSNP → 6295. The table shows each extracted connection, where it came from and its confidence.
| Subject | Predicate | Object | Confidence | Src |
|---|---|---|---|---|
| Rs6295 | Chromosome | 5 | 1.00 | infobox |
| Rs6295 | dbSNP | 6295 | 1.00 | infobox |
| Rs6295 | Ensembl | Human SNPView | 1.00 | infobox |
| Rs6295 | Gene | HTR1A | 1.00 | infobox |
| Rs6295 | HapMap | 6295 | 1.00 | infobox |
| Rs6295 | Name(s) | C-1019G, C(-1019)G | 1.00 | infobox |
| Rs6295 | Region | Promoter | 1.00 | infobox |
| Rs6295 | SNPedia | 6295 | 1.00 | infobox |
The concept neighborhoods around Rs6295 bring nearby vocabulary together. In this analysis, examples include Nucleotide, Single and Variation. Use the clusters to find adjacent concepts and terminology that may deserve separate research.
For Rs6295, one of the stronger structural bridges in this analysis connects Rs6295 with Overview. Bridges highlight paths between different parts of the map and can reveal research angles that are easy to miss in a flat list.
TTTA analyzes the structure around Rs6295 to surface related topics, entities, relationships, concept neighborhoods and bridge connections. Use the map to explore areas such as Regions, Personality & Disorders, including less central topics that may reveal useful research gaps. Automatically extracted connections are research leads rather than rewritten encyclopedia content.
Source: Wikipedia — Rs6295 · EN edition · Analysis: TopicsToTalkAbout