Source: CURATED ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs13361160
rs13361160 		C 0.800 GeneticVariation GWASCAT Genome-wide association study meta-analysis of chronic widespread pain: evidence for involvement of the 5p15.2 region. 22956598

2013
dbSNP: rs13361160
rs13361160 		C 0.800 GeneticVariation GWASDB Genome-wide association study meta-analysis of chronic widespread pain: evidence for involvement of the 5p15.2 region. 22956598

2013
dbSNP: rs17122021
rs17122021 		0.800 GeneticVariation GWASCAT Genome-wide association study of acute post-surgical pain in humans. 19207018

2009
dbSNP: rs17122021
rs17122021 		0.800 GeneticVariation GWASDB Genome-wide association study of acute post-surgical pain in humans. 19207018

2009
dbSNP: rs2562456
rs2562456
LINC00664
0.800 GeneticVariation GWASCAT Genome-wide association study of acute post-surgical pain in humans. 19207018

2009
dbSNP: rs2562456
rs2562456
LINC00664
0.800 GeneticVariation GWASDB Genome-wide association study of acute post-surgical pain in humans. 19207018

2009
dbSNP: rs1972597
rs1972597 		G 0.700 GeneticVariation GWASCAT Genome-wide association study suggests common variants within RP11-634B7.4 gene influencing severe pre-treatment pain in head and neck cancer patients. 27670397

2016
dbSNP: rs3862188
rs3862188 		G 0.700 GeneticVariation GWASCAT We identified 3 common genetic variants in high linkage disequilibrium for severe pre-treatment pain, representing one genomic region at 1q44 (rs3862188, P = 3.45 × 10<sup>-8</sup>; rs880143, P = 3.45 × 10<sup>-8</sup>; and rs7526880, P = 4.92 × 10<sup>-8</sup>), which maps to the RP11-634B7.4 gene, a novel antisense gene to three olfactory receptor genes. 27670397

2016
dbSNP: rs1057518927
rs1057518927
OAT
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1057518946
rs1057518946
GJB1
T 0.700 GeneticVariation CLINVAR

dbSNP: rs121908552
rs121908552
SCN4A ; LOC105371858
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1445287184
rs1445287184
PTPRQ ; LOC105369867
T 0.700 CausalMutation CLINVAR

dbSNP: rs1554781700
rs1554781700
COL5A1
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1555735545
rs1555735545
STRN4 ; FKRP
A 0.700 CausalMutation CLINVAR

dbSNP: rs28937900
rs28937900
FKRP
A 0.700 CausalMutation CLINVAR

dbSNP: rs397514698
rs397514698
GNAQ
T 0.700 CausalMutation CLINVAR

dbSNP: rs781565158
rs781565158
PYROXD1
G 0.700 CausalMutation CLINVAR