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rs17122021

From SNPedia

Orientationplus
Stabilizedplus
Make rs17122021(C;C)
Make rs17122021(C;T)
Make rs17122021(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position118274971
is asnp
is mentioned by
dbSNPrs17122021
ebirs17122021
HLIrs17122021
Exacrs17122021
Varsomers17122021
Maprs17122021
PheGenIrs17122021
hapmaprs17122021
1000 genomesrs17122021
hgdprs17122021
ensemblrs17122021
gopubmedrs17122021
geneviewrs17122021
scholarrs17122021
googlers17122021
pharmgkbrs17122021
gwascentralrs17122021
openSNPrs17122021
23andMers17122021
23andMe allrs17122021
SNP Nexus

SNPshotrs17122021
SNPdbers17122021
MSV3drs17122021
GWAS Ctlgrs17122021
GMAF0.4399
Max Magnitude
? (C;C) (C;T) (T;T) 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 7E-7
Odds Ratio NR NR



GET Evidence
rs17122021
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.382812
summary