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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.
Regions, Personality & Disorders
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gene g-allele one study snp htr1a snps association studies polymorphism investigated disorders personality -1019 human found disorder also among caucasian
| 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 |
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