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- Rs6295 abstract "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 effect of the SNP on the binding potential of the human 5-HT1A neuroreceptor has been assessed with positron emission tomography and the WAY-100635 radioligand, with a study reporting no apparent influence from the SNP.".
- Rs6295 wikiPageID "17870559".
- Rs6295 wikiPageRevisionID "574810451".
- Rs6295 chromosome "5".
- Rs6295 gene "HTR1A".
- Rs6295 hasPhotoCollection Rs6295.
- Rs6295 name "C-1019G".
- Rs6295 name "CG".
- Rs6295 personalitystudyGenotype "G".
- Rs6295 personalitystudyInventory "NEO PI-R".
- Rs6295 personalitystudyInventory "TPQ".
- Rs6295 personalitystudyPmid "14666415".
- Rs6295 personalitystudyTrait "Harm Avoidance".
- Rs6295 personalitystudyTrait "Neuroticism".
- Rs6295 region "Promoter".
- Rs6295 rsid "6295".
- Rs6295 subject Category:Single-nucleotide_polymorphisms.
- Rs6295 comment "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 effect of the SNP on the binding potential of the human 5-HT1A neuroreceptor has been assessed with positron emission tomography and the WAY-100635 radioligand, with a study reporting no apparent influence from the SNP.".
- Rs6295 label "Rs6295".
- Rs6295 sameAs m.047fytm.
- Rs6295 sameAs Q7375575.
- Rs6295 sameAs Q7375575.
- Rs6295 wasDerivedFrom Rs6295?oldid=574810451.
- Rs6295 isPrimaryTopicOf Rs6295.