{{Rsnum
|rsid=6693882
|Chromosome=1
|position=95680412
|Orientation=plus
|GMAF=0.3131
|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 | 23.0 | 51.3 | 25.7
| HCB | 58.4 | 30.7 | 10.9
| JPT | 69.0 | 27.4 | 3.5
| YRI | 96.6 | 3.4 | 0.0
| ASW | 68.4 | 31.6 | 0.0
| CHB | 58.4 | 30.7 | 10.9
| CHD | 57.8 | 34.9 | 7.3
| GIH | 25.7 | 49.5 | 24.8
| LWK | 89.1 | 10.0 | 0.9
| MEX | 53.4 | 36.2 | 10.3
| MKK | 65.4 | 34.0 | 0.6
| TSI | 34.3 | 40.2 | 25.5
| HapMapRevision=28
}}
{{PMID Auto GWAS
|PMID=19207018
|Trait=Pain
|Title=Genome-wide association study of acute post-surgical pain in humans
|RiskAllele=
|Pval=0.000002
|OR=NR
|ORtxt=NR
|OA=1
}}

{{PharmGKB
|RSID=rs6693882
|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: 1p21.3; Reported Gene(s): NR; Risk Allele: rs6693882-?); (p-value= 0.000002).This variant is associated with Pain.
|Drugs=
|Drug Classes=
|Diseases=Pain
|Curation Level=Non-Curated
|PharmGKB Accession ID=PA164739990
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs6693882
|overall_frequency_n=34
|overall_frequency_d=128
|overall_frequency=0.265625
|n_genomes=19
|n_genomes_annotated=0
|n_haplomes=26
|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}}