Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2701448
rs2701448
Entrez Id: 8989;100132891
Gene Symbol: TRPA1;MSC-AS1
TRPA1;MSC-AS1
CUI: C0233849
Disease:
Personality Traits
A 0.700 GeneticVariation GWASDB Genome-wide association study of personality traits in the long life family study. 23658558 2013
dbSNP: rs398123010
rs398123010
Entrez Id: 8989;100132891
Gene Symbol: TRPA1;MSC-AS1
TRPA1;MSC-AS1
CUI: C3808667
Disease:
EPISODIC PAIN SYNDROME, FAMILIAL, 1
0.700 GeneticVariation UNIPROT A gain-of-function mutation in TRPA1 causes familial episodic pain syndrome. 20547126 2010
dbSNP: rs920829
rs920829
Entrez Id: 8989;100132891
Gene Symbol: TRPA1;MSC-AS1
TRPA1;MSC-AS1
CUI: C0002895
Disease:
Anemia, Sickle Cell
0.010 GeneticVariation BEFREE We identified that rs920829 (incident rate ratio = 1.44, p = 0.027 additive; IRR=1.68, p=0.008 recessive models of negative binomial regression) and the CGAGG haplotype of TRPA1 (odds ratio = 0.218, p = 0.009) were significantly associated with utilization rate, suggesting that TRPA1 gene polymorphisms may influence acute pain crisis in SCD. 29620434 2018
dbSNP: rs1384001
rs1384001
Entrez Id: 8989;100132891
Gene Symbol: TRPA1;MSC-AS1
TRPA1;MSC-AS1
CUI: C0004096
Disease:
Asthma
0.010 GeneticVariation BEFREE In ALSPAC, there was strong evidence for association between six SNPs and asthma: rs959974 and rs1384001 (per-allele odds ratio for both: 1.30 (95% CI: 1.15-1.47), p = 0.00001), rs7010969 (OR 1.28 (1.13-1.46), p = 0.00004), rs3735945 (OR 1.30 (1.09-1.55), p = 0.003), rs920829 (OR 1.30 (1.09-1.54), p = 0.004) and rs4738202 (OR 1.22 (1.07-1.39), p = 0.004). 27779810 2017
dbSNP: rs3735945
rs3735945
Entrez Id: 8989;100132891
Gene Symbol: TRPA1;MSC-AS1
TRPA1;MSC-AS1
CUI: C0004096
Disease:
Asthma
0.010 GeneticVariation BEFREE In ALSPAC, there was strong evidence for association between six SNPs and asthma: rs959974 and rs1384001 (per-allele odds ratio for both: 1.30 (95% CI: 1.15-1.47), p = 0.00001), rs7010969 (OR 1.28 (1.13-1.46), p = 0.00004), rs3735945 (OR 1.30 (1.09-1.55), p = 0.003), rs920829 (OR 1.30 (1.09-1.54), p = 0.004) and rs4738202 (OR 1.22 (1.07-1.39), p = 0.004). 27779810 2017
dbSNP: rs4738202
rs4738202
Entrez Id: 8989;100132891
Gene Symbol: TRPA1;MSC-AS1
TRPA1;MSC-AS1
CUI: C0004096
Disease:
Asthma
0.010 GeneticVariation BEFREE In ALSPAC, there was strong evidence for association between six SNPs and asthma: rs959974 and rs1384001 (per-allele odds ratio for both: 1.30 (95% CI: 1.15-1.47), p = 0.00001), rs7010969 (OR 1.28 (1.13-1.46), p = 0.00004), rs3735945 (OR 1.30 (1.09-1.55), p = 0.003), rs920829 (OR 1.30 (1.09-1.54), p = 0.004) and rs4738202 (OR 1.22 (1.07-1.39), p = 0.004). 27779810 2017
dbSNP: rs7010969
rs7010969
Entrez Id: 8989;100132891
Gene Symbol: TRPA1;MSC-AS1
TRPA1;MSC-AS1
CUI: C0004096
Disease:
Asthma
0.010 GeneticVariation BEFREE In ALSPAC, there was strong evidence for association between six SNPs and asthma: rs959974 and rs1384001 (per-allele odds ratio for both: 1.30 (95% CI: 1.15-1.47), p = 0.00001), rs7010969 (OR 1.28 (1.13-1.46), p = 0.00004), rs3735945 (OR 1.30 (1.09-1.55), p = 0.003), rs920829 (OR 1.30 (1.09-1.54), p = 0.004) and rs4738202 (OR 1.22 (1.07-1.39), p = 0.004). 27779810 2017
dbSNP: rs920829
rs920829
Entrez Id: 8989;100132891
Gene Symbol: TRPA1;MSC-AS1
TRPA1;MSC-AS1
CUI: C0004096
Disease:
Asthma
0.010 GeneticVariation BEFREE In ALSPAC, there was strong evidence for association between six SNPs and asthma: rs959974 and rs1384001 (per-allele odds ratio for both: 1.30 (95% CI: 1.15-1.47), p = 0.00001), rs7010969 (OR 1.28 (1.13-1.46), p = 0.00004), rs3735945 (OR 1.30 (1.09-1.55), p = 0.003), rs920829 (OR 1.30 (1.09-1.54), p = 0.004) and rs4738202 (OR 1.22 (1.07-1.39), p = 0.004). 27779810 2017
dbSNP: rs959974
rs959974
Entrez Id: 8989;100132891
Gene Symbol: TRPA1;MSC-AS1
TRPA1;MSC-AS1
CUI: C0004096
Disease:
Asthma
0.010 GeneticVariation BEFREE In ALSPAC, there was strong evidence for association between six SNPs and asthma: rs959974 and rs1384001 (per-allele odds ratio for both: 1.30 (95% CI: 1.15-1.47), p = 0.00001), rs7010969 (OR 1.28 (1.13-1.46), p = 0.00004), rs3735945 (OR 1.30 (1.09-1.55), p = 0.003), rs920829 (OR 1.30 (1.09-1.54), p = 0.004) and rs4738202 (OR 1.22 (1.07-1.39), p = 0.004). 27779810 2017
dbSNP: rs11988795
rs11988795
Entrez Id: 8989;100132891
Gene Symbol: TRPA1;MSC-AS1
TRPA1;MSC-AS1
CUI: C0030193
Disease:
Pain
0.010 GeneticVariation BEFREE Olfactory function and nociception was compared between carriers (n = 38) and non-carriers (n = 43) of TRPA1 variant rs11988795 G>A, a variant known to enhance cold pain perception. 24752136 2014
dbSNP: rs200192163
rs200192163
Entrez Id: 8989;100132891
Gene Symbol: TRPA1;MSC-AS1
TRPA1;MSC-AS1
CUI: C0030193
Disease:
Pain
0.010 GeneticVariation BEFREE Human TRPM8 and TRPA1 pain channels, including a gene variant with increased sensitivity to agonists (TRPA1 R797T), exhibit differential regulation by SRC-tyrosine kinase inhibitor. 24975826 2014
dbSNP: rs398123010
rs398123010
Entrez Id: 8989;100132891
Gene Symbol: TRPA1;MSC-AS1
TRPA1;MSC-AS1
CUI: C1611743
Disease:
Familial (FPAH)
0.010 GeneticVariation BEFREE Remarkably, a substitution of single amino acid in the S4-S5 region of TRPA1 (N855S) has been recently associated with familial episodic pain syndrome. 24564660 2014
dbSNP: rs398123010
rs398123010
Entrez Id: 8989;100132891
Gene Symbol: TRPA1;MSC-AS1
TRPA1;MSC-AS1
CUI: C0391976
Disease:
Pain Disorder
0.010 GeneticVariation BEFREE Remarkably, a substitution of single amino acid in the S4-S5 region of TRPA1 (N855S) has been recently associated with familial episodic pain syndrome. 24564660 2014
dbSNP: rs920829
rs920829
Entrez Id: 8989;100132891
Gene Symbol: TRPA1;MSC-AS1
TRPA1;MSC-AS1
CUI: C0085625
Disease:
Hypoalgesia
0.010 GeneticVariation BEFREE However, in neuropathic pain patients transient receptor potential ankyrin 1 710G>A (rs920829, E179K) was associated with the presence of paradoxical heat sensation (p = 0.03), and transient receptor potential vanilloid 1 1911A>G (rs8065080, I585V) with cold hypoalgesia (p = 0.0035). 21468319 2011