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rs6693882

From SNPedia

Orientationplus
Stabilizedplus
Make rs6693882(A;A)
Make rs6693882(A;G)
Make rs6693882(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position95680412
is asnp
is mentioned by
dbSNPrs6693882
ebirs6693882
HLIrs6693882
Exacrs6693882
Varsomers6693882
Maprs6693882
PheGenIrs6693882
hapmaprs6693882
1000 genomesrs6693882
hgdprs6693882
ensemblrs6693882
gopubmedrs6693882
geneviewrs6693882
scholarrs6693882
googlers6693882
pharmgkbrs6693882
gwascentralrs6693882
openSNPrs6693882
23andMers6693882
23andMe allrs6693882
SNP Nexus

SNPshotrs6693882
SNPdbers6693882
MSV3drs6693882
GWAS Ctlgrs6693882
GMAF0.3131
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 19207018OA-icon.png]
Trait Pain
Title Genome-wide association study of acute post-surgical pain in humans
Risk Allele
P-val 0.000002
Odds Ratio NR NR



GET Evidence
rs6693882
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.265625
summary