Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs61816761
rs61816761
CUI: C0013595
Disease: Eczema
Eczema
A 0.900 CausalMutation CLINVAR

dbSNP: rs886041094
rs886041094
CUI: C0013595
Disease: Eczema
Eczema
A 0.700 GeneticVariation CLINVAR

dbSNP: rs886039903
rs886039903
CUI: C0013595
Disease: Eczema
Eczema
T 0.700 CausalMutation CLINVAR

dbSNP: rs780533096
rs780533096
CUI: C0013595
Disease: Eczema
Eczema
T 0.700 GeneticVariation CLINVAR

dbSNP: rs759191907
rs759191907
CUI: C0013595
Disease: Eczema
Eczema
G 0.700 CausalMutation CLINVAR

dbSNP: rs397514698
rs397514698
CUI: C0013595
Disease: Eczema
Eczema
T 0.700 CausalMutation CLINVAR

dbSNP: rs387906760
rs387906760
CUI: C0013595
Disease: Eczema
Eczema
T 0.700 CausalMutation CLINVAR

dbSNP: rs374052333
rs374052333
CUI: C0013595
Disease: Eczema
Eczema
T 0.700 GeneticVariation CLINVAR

dbSNP: rs200473652
rs200473652
CUI: C0013595
Disease: Eczema
Eczema
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1555549674
rs1555549674
CUI: C0013595
Disease: Eczema
Eczema
G 0.700 CausalMutation CLINVAR

dbSNP: rs1555548678
rs1555548678
CUI: C0013595
Disease: Eczema
Eczema
A 0.700 CausalMutation CLINVAR

dbSNP: rs1555483699
rs1555483699
CUI: C0013595
Disease: Eczema
Eczema
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1554236040
rs1554236040
CUI: C0013595
Disease: Eczema
Eczema
T 0.700 CausalMutation CLINVAR

dbSNP: rs114925667
rs114925667
CUI: C0013595
Disease: Eczema
Eczema
A 0.700 CausalMutation CLINVAR

dbSNP: rs555743307
rs555743307
CUI: C0013595
Disease: Eczema
Eczema
0.040 GeneticVariation BEFREE To assess whether genetic variants of TXA2 receptor, IL-4 and IL-4R alpha genes relate to the elevation of serum immunoglobulin E levels in patients with atopic dermatitis (AD), we conducted an association study of genetic polymorphisms of TXA2 receptor (795C/T), IL-4 (-589C/T), and IL-4R alpha (Ile50Val) in a Japanese population (n = 789). 11922633

2002

dbSNP: rs2303067
rs2303067
CUI: C0013595
Disease: Eczema
Eczema
0.070 GeneticVariation BEFREE These results suggest that SPINK5 Glu420Lys polymorphism may be associated with certain asthma phenotypes characterized by the concomitant expression of asthma and atopic dermatitis or SPT reactivity. 15005725

2004

dbSNP: rs2228428
rs2228428
CUI: C0013595
Disease: Eczema
Eczema
0.010 GeneticVariation BEFREE C1014T SNP of CCR4 does not appear to be associated with susceptibility to atopic dermatitis in Japanese patients. 15202833

2004

dbSNP: rs2303067
rs2303067
CUI: C0013595
Disease: Eczema
Eczema
0.070 GeneticVariation BEFREE We investigated whether single nucleotide polymorphisms in SPINK5 (ie, -785 A/G, Asn368Ser, and Lys420Glu) are associated with asthma, atopic phenotypes, and atopic dermatitis in 200 families ascertained by a proband with asthma (nonaffected spouses served as a matched control population) and an independent set of 252 trios with asthma. 15753894

2005

dbSNP: rs2303063
rs2303063
CUI: C0013595
Disease: Eczema
Eczema
0.020 GeneticVariation BEFREE We investigated whether single nucleotide polymorphisms in SPINK5 (ie, -785 A/G, Asn368Ser, and Lys420Glu) are associated with asthma, atopic phenotypes, and atopic dermatitis in 200 families ascertained by a proband with asthma (nonaffected spouses served as a matched control population) and an independent set of 252 trios with asthma. 15753894

2005

dbSNP: rs2303067
rs2303067
CUI: C0013595
Disease: Eczema
Eczema
0.070 GeneticVariation BEFREE The Glu420Lys variant showed significant association with atopy, asthma and atopic dermatitis in recent studies. 15820494

2005

dbSNP: rs2569193
rs2569193
CUI: C0013595
Disease: Eczema
Eczema
0.010 GeneticVariation BEFREE In dominant models adjusted for potential confounders, SNP rs2569193 was associated with significantly decreased risk for eczema (odds ratio [OR] for CT/TT vs CC, 0.5; 95% CI, 0.3-0.8), whereas SNP rs2569190 (also reported as the C-159T) was associated with significantly increased risk for eczema (OR for CT/TT vs CC, 2.3; 95% CI, 1.4-3.8). 15867866

2005

dbSNP: rs2569190
rs2569190
CUI: C0013595
Disease: Eczema
Eczema
0.010 GeneticVariation BEFREE In dominant models adjusted for potential confounders, SNP rs2569193 was associated with significantly decreased risk for eczema (odds ratio [OR] for CT/TT vs CC, 0.5; 95% CI, 0.3-0.8), whereas SNP rs2569190 (also reported as the C-159T) was associated with significantly increased risk for eczema (OR for CT/TT vs CC, 2.3; 95% CI, 1.4-3.8). 15867866

2005

dbSNP: rs436857
rs436857
CUI: C0013595
Disease: Eczema
Eczema
0.010 GeneticVariation BEFREE In a case-control association study, we found that promoter polymorphisms -111A/T and -2C/T were significantly associated with an increased risk of AD under a recessive model. 16159888

2005

dbSNP: rs5743810
rs5743810
CUI: C0013595
Disease: Eczema
Eczema
0.010 GeneticVariation BEFREE Genotyping of the Ser249Pro polymorphism in 68 unrelated adult patients and 132 unrelated children with asthma, 185 unrelated patients with COPD, 295 unrelated individuals with AD and 212 healthy control subjects was performed by restriction enzyme digestion. 16188043

2005

dbSNP: rs895691
rs895691
CUI: C0013595
Disease: Eczema
Eczema
0.010 GeneticVariation BEFREE In the MRC-E panel, rs895691, between the end of exon 6 of SLC9A3R1 and exon 7 of NAT9, was associated with AD (P = 0.037). 16374479

2006