{{Rsnum
|rsid=2705293
|Gene=FLJ45872
|Chromosome=8
|position=137906702
|Orientation=minus
|GMAF=0.1157
|Gene_s=TRDJ1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 85.7 | 14.3 | 0.0
| HCB | 85.4 | 14.6 | 0.0
| JPT | 91.2 | 8.0 | 0.9
| YRI | 57.1 | 36.7 | 6.1
| ASW | 57.9 | 33.3 | 8.8
| CHB | 85.4 | 14.6 | 0.0
| CHD | 95.4 | 4.6 | 0.0
| GIH | 90.1 | 9.9 | 0.0
| LWK | 47.3 | 43.6 | 9.1
| MEX | 89.7 | 10.3 | 0.0
| MKK | 55.8 | 36.5 | 7.7
| TSI | 85.3 | 13.7 | 1.0
| HapMapRevision=28
}}
[[rs9291683]], [[rs3129934]] and [[rs2705293]] discussed in the context of [[CNV]]s in a [https://sites.google.com/a/codushlaine.com/colm-o-dushlaine/23andcolm/day14-cnvs blog post]

{{GWAS Summary
|SNP=rs2705293
|PubMedID=18762592
|Condition=Neuroticism
|Gene=AK127771
|Risk Allele=
|pValue=6.00E-006
|OR=NA
|95CI=
}}

{{PharmGKB
|RSID=rs2705293
|Name_s=
|Gene_s=-
|Feature=
|Evidence=PubMed ID:18762592; Web Resource:http://www.genome.gov/gwastudies/
|Annotation=GWAS results: Genomewide Association Analysis Followed by a Replication Study Implicates a Novel Candidate Gene for Neuroticism (Initial Sample Size: 1,227 individuals; Replication Sample Size: 1,880 individuals). This variant is associated with Neuroticism.
|Drugs=
|Drug Classes=
|Diseases=
|Curation Level=Non-Curated
|PharmGKB Accession ID=PA162356456
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs2705293
|overall_frequency_n=106
|overall_frequency_d=128
|overall_frequency=0.828125
|n_genomes=53
|n_genomes_annotated=0
|n_haplomes=89
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|in_pharmgkb=Y
|autoscore=2
|webscore=N
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | HumanOmni1Quad}}