Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1555206402
rs1555206402
HMBS
A 0.700 CausalMutation CLINVAR

dbSNP: rs1555640521
rs1555640521
LAMA1
G 0.700 GeneticVariation CLINVAR

dbSNP: rs886037774
rs886037774
LPL
C 0.700 GeneticVariation CLINVAR

dbSNP: rs886037775
rs886037775
LPL
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1799971
rs1799971
OPRM1
0.020 GeneticVariation BEFREE OPRM1-A118G polymorphism (A > G) is associated with a reduced risk of postoperative vomiting, but not nausea, pruritus and dizziness. 30323865

2018
dbSNP: rs1799971
rs1799971
OPRM1
0.020 GeneticVariation BEFREE A total of 207 patients were screened for A118G and randomly received different combinations of propofol and remifentanil, changed depending on the nausea response to endoscopy tube introduction. 23503369

2013
dbSNP: rs349358
rs349358
KCNB2
0.010 GeneticVariation BEFREE Early PONV occurred in 37%.There was a significant association of the KCNB2 rs349358 SNP with nausea (P = 0.021), retching (P = 0.001), and PONV (P = 0.006). 31077873

2020
dbSNP: rs1695
rs1695
GSTP1
0.010 GeneticVariation BEFREE GSTP1 c.313A>G genotyping may reduce the use of preventive support for chemotherapy induced nausea and lower the overall cost of treatment. 30870506

2019
dbSNP: rs2231142
rs2231142
ABCG2
0.010 GeneticVariation BEFREE Multivariate logistic regression analysis revealed that the ABCG2 (rs2231142) AA genotype is significantly associated with acute significant nausea (odds ratio, 4.87; 95% confidence interval, 1.01-23.60; P = .049). 28735677

2018
dbSNP: rs6313
rs6313
HTR2A
0.010 GeneticVariation BEFREE The relationship between the serotonin 2A receptor gene -1438A/G and 102T/C polymorphisms and citalopram/sertraline-induced nausea in major depressed patients. 30221791

2018
dbSNP: rs150283105
rs150283105
ACAD9 ; KIAA1257
0.010 GeneticVariation BEFREE We report a 36-year-old female having lifetime exercise intolerance and lactic acidosis with nausea associated with novel compound heterozygous Acyl-CoA dehydrogenase 9 gene (ACAD9) mutations (p.Ala390Thr and p.Arg518Cys). 28279569

2017
dbSNP: rs763004980
rs763004980
ACAD9
0.010 GeneticVariation BEFREE We report a 36-year-old female having lifetime exercise intolerance and lactic acidosis with nausea associated with novel compound heterozygous Acyl-CoA dehydrogenase 9 gene (ACAD9) mutations (p.Ala390Thr and p.Arg518Cys). 28279569

2017
dbSNP: rs6806362
rs6806362 		0.010 GeneticVariation BEFREE After adjustment for these two parameters, the two SNPs rs6806362 (odds ratio (OR) 1.38 per allele; 95% confidence interval (CI) 1.06-1.79; p = 0.017) and rs6807670 (OR 1.37; 95% CI 1.05-1.79 per allele; p = 0.023) were marginally associated with pregnancy-related nausea. 20021265

2010
dbSNP: rs6807670
rs6807670
HTR3C
0.010 GeneticVariation BEFREE After adjustment for these two parameters, the two SNPs rs6806362 (odds ratio (OR) 1.38 per allele; 95% confidence interval (CI) 1.06-1.79; p = 0.017) and rs6807670 (OR 1.37; 95% CI 1.05-1.79 per allele; p = 0.023) were marginally associated with pregnancy-related nausea. 20021265

2010
dbSNP: rs1176744
rs1176744
HTR3B
0.010 GeneticVariation BEFREE The Tyr129Ser polymorphism of the HTR3B gene had a significant effect on the incidence of nausea (P=0.038). 16534507

2006