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rs2770296

From SNPedia

Orientationplus
Stabilizedplus
Make rs2770296(C;C)
Make rs2770296(C;T)
Make rs2770296(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position46866425
GeneHTR2A
is asnp
is mentioned by
dbSNPrs2770296
ebirs2770296
HLIrs2770296
Exacrs2770296
Varsomers2770296
Maprs2770296
PheGenIrs2770296
hapmaprs2770296
1000 genomesrs2770296
hgdprs2770296
ensemblrs2770296
gopubmedrs2770296
geneviewrs2770296
scholarrs2770296
googlers2770296
pharmgkbrs2770296
gwascentralrs2770296
openSNPrs2770296
23andMers2770296
23andMe allrs2770296
SNP Nexus

SNPshotrs2770296
SNPdbers2770296
MSV3drs2770296
GWAS Ctlgrs2770296
GMAF0.2342
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 19584773] Association between the serotonin 2A receptor gene and bipolar affective disorder in an Australian cohort

"Haplotype association analysis suggests that the haplotype CCGCA (at SNPs rs3125, rs6314, rs1923886, rs2224721 and rs2770296) is protective against bipolar disorder (P = 0.021, odds ratio 0.63) and the rarer haplotype CCACG confers risk to the disorder (P = 0.0065, odds ratio 3.08)."


[PMID 19566713] Investigation of 17 candidate genes for personality traits confirms effects of the HTR2A gene on novelty seeking


[PMID 18712714OA-icon.png] Genetic variation in the serotonin 2A receptor and suicidal ideation in a sample of 270 Irish high-density schizophrenia families.


[PMID 19184136OA-icon.png] Examination of association of genes in the serotonin system to autism.


[PMID 22947179] Analysis of 34 candidate genes in bupropion and placebo remission