{{Rsnum
|rsid=17122021
|Chromosome=11
|position=118274971
|Orientation=plus
|GMAF=0.4399
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 30.1 | 45.1 | 24.8
| HCB | 19.7 | 52.6 | 27.7
| JPT | 29.2 | 45.1 | 25.7
| YRI | 53.7 | 38.8 | 7.5
| ASW | 45.6 | 40.4 | 14.0
| CHB | 19.7 | 52.6 | 27.7
| CHD | 20.2 | 49.5 | 30.3
| GIH | 20.8 | 54.5 | 24.8
| LWK | 34.5 | 58.2 | 7.3
| MEX | 36.2 | 48.3 | 15.5
| MKK | 55.1 | 38.5 | 6.4
| TSI | 34.3 | 45.1 | 20.6
| HapMapRevision=28
}}
{{PMID Auto GWAS
|PMID=19207018
|Trait=Pain
|Title=Genome-wide association study of acute post-surgical pain in humans
|RiskAllele=
|Pval=7E-7
|OR=NR
|ORtxt=NR
|OA=1
}}

{{PharmGKB
|RSID=rs17122021
|Name_s=
|Gene_s=-
|Feature=
|Evidence=PubMed ID:19207018; Web Resource:http://www.genome.gov/gwastudies/
|Annotation=GWAS results: Genome-wide association study of acute post-surgical pain in humans. (Initial Sample Size: 60 females, 52 males; Replication Sample Size: NR); (Region: 11q23.3; Reported Gene(s): NR; Risk Allele: rs17122021-?); (p-value= 0.0000007).This variant is associated with Pain.
|Drugs=
|Drug Classes=
|Diseases=Pain
|Curation Level=Non-Curated
|PharmGKB Accession ID=PA164739991
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs17122021
|overall_frequency_n=49
|overall_frequency_d=128
|overall_frequency=0.382812
|n_genomes=37
|n_genomes_annotated=0
|n_haplomes=44
|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}}