Browse Result

Total number of records for in F of in DAAB (Version-2) database: 43

Record no	GENE NAME	SNP ID	CHANGES	ANCESTRAL ALLELES	FUNCTIONAL CONSEQUENCES	DISEASE	POPULATION	Pubmed ID	Comments
1	FOXP3	rs56066773	C/T	C	3' Untranslated Region	Atopy and Autoimmunity	Caucasian individuals	25982578	The mutated allele of 7340C>T was significantly associated with the simultaneous presence of autoimmunity and atopy in male children, but not those that only suffered from one disease.
2	FOXP3	rs2232367	C/T	C	Coding region of Exon 5	Atopy and Autoimmunity	Caucasian individuals	25982578	A significant increase in the frequency of the mutated allele of 1651C>T in the male control group as compared to patients with atopy and autoimmunity.
3	FCER1B	rs2583476	C/T	T	Intron Variant	Asthma	Pakistani population	29588858	For FCER1B gene, rs2583476 the asthmatic male gender had higher TT genotype counts as compared to controls.
4	FLG	rs11204981	A/G	A	2KB Upstream Variant	Eczema plus Asthma phenotype	-	29569866	SNP in FLG (rs11204981) may serve as an important predictive marker for the combined eczema plus asthma phenotype and the highest level of expression in heterozygous may have a protective role in developing allergy phenotype.
5	FAM167A-BLK	rs2254546	A/G	G	-	Childhood Asthma	Han Chinese population	27088737	FAM167A-BLK (rs2254546) was significantly correlated with Asthma and Allergic Rhinitis. With regard to rs2254546, the AA and AG genotypes and the A allele decreased the risk of asthma with comorbid AR.
6	FAM167A-BLK	rs1600249	T/G	T	Intron Variant	Childhood Asthma	Han Chinese population	27088737	FAM167A-BLK (rs1600249) was significantly correlated with Asthma and Allergic Rhinitis. For rs1600249, the A A and AC genotypes and the A allele were protective factors for asthma with comorbid AR. SNP rsl600249 was associated with asthma without allergic rhinitis as a risk factor.
7	FCER1B	rs569108	C/T	T	Missense Variant	Childhood Asthma	Chinese Han population	26613553	Individuals homozygous for the risk alleles (GG) for rs569108 are at a higher risk for developing asthma compared with those without any risk homozygotes. IL13 rs20541 (G allele), IL4 rs2243250 (T allele), ADRB2 rs1042713 (A allele), and FCER1B rs569108 (G allele), four SNPs with significant sole effect on asthma, interact to confer a higher risk for the disease in Chinese Han children.
8	FCER1B	rs569108	C/T(REV)	T	Missense Variant	Asthma	Asian population	28865417	In stratified analysis on the basis of atopic status, a significant increased atopic asthma risk was observed under the allelic genetic model, implying that FCER1B 237G-allele carriers have a 34.9% enhanced risk of atopic asthma compared with 237E-allele carriers. A marginally significant association between FCER1B E237G polymorphism and atopic asthma risk was noted under the dominant genetic model.
9	FCER1B	-	-	-	-	Asthma	East Asian population	28865417	A significantly elevated asthma risk was associated with FCER1B C-108T allele in the East Asian population when summarizing the studies from China, South Korea and Japan.
10	FOXO3	rs13217795	C/T	C	Intron Variant	Asthma, Allergic Rhinitis	Arabian population	29141605	An association was observed between rs13217795 and allergic rhinitis. This study also presented the first independent verification of the association between rs13217795 and asthma.
11	FCRL5	rs6692977	C/G/T	C	Intron Variant	Asthma, Allergic Rhinitis	Chinese Han population	30771554	The frequencies of the rs6692977 CT genotype and T allele within FCRL5 were significantly higher in Asthma with comorbid Allergic Rhinitis compared to healthy controls.
12	FCRL3	rs7528684	A/G	G	2KB Upstream Variant	Asthma, Allergic Rhinitis	Chinese Han population	30771554	The frequency of the rs7528684 A allele within FCRL3 was higher in Asthma with comorbid Allergic Rhinitis than in controls.
13	FCRL3	rs10489678	A/C/G/T	G	Intron Variant	Asthma, Allergic Rhinitis	Chinese Han population	30771554	The frequency of the rs10489678 G allele within FCRL3 was higher in Asthma with comorbid Allergic Rhinitis than in controls.
14	FAM71A	rs147978008	-	-	2KB Upstream Variant (Deletion)	Diisocyanate Induced Asthma	European population	29969634	rs147978008, associated with Diisocyanate Induced Asthma is considered most likely to function by altering gene regulatory mechanism in disease relevant cells.
15	FAM71A, Loc100129948	rs17019510	A/G	G	Intergenic Variant	Diisocyanate Induced Asthma	European population	29969634	rs17019510, associated with Diisocyanate Induced Asthma is considered most likely to function by altering gene regulatory mechanism in disease relevant cells.
16	FZD6	rs3133835	A/G	G	-	Asthma	Spanish population	28079285	This SNP was associated with the risk of asthma susceptibility .
17	FZD6	rs3133836	C/T	T	-	Asthma	Spanish population	28079285	This SNP was associated with the risk of asthma susceptibility .
18	FZD6	rs3133805	G/T	T	-	Asthma	Spanish population	28079285	The minor allele (G allele) of rs3133805 was associated with the risk of asthma susceptibility.
19	FCER1B	rs569108	C/T	T	Missense Variant	Asthma, Atopy	Chinese Han population	29761786	FCER1B rs569108 was associated with the Asthma Predictive Index (API) and atopy.
20	FLG	rs61816761	A/G/T	G	Stop Gained	Multiple Contact Allergies	North American population	30868611	There was a significant association between R501X mutation (rs61816761) and polysensitivity.
21	FCER2	rs28364072	A/G	-	Intron Variant	Asthma	Vietnamese population	27695350	The concentration of FENO in homozygous variant rs28364072 (CC) of FCER2 gene was significantly higher than homozygous wild type (TT) and heterozygous (TC).
22	FLG	rs145627745	A/T	A	Missense Variant	Non Allergic Asthma	Spanish population	27462351	The 1741A > T (rs145627745) polymorphism seems to be associated with non-allergic asthma.
23	FCER1B	-	-	-	-	Allergic Disease (Asthma, Allergic Rhinitis)	-	29654163	FCER1B -109C/T polymorphism may serve as risk factor for allergic diseases.
24	FCER1B	rs569108	C/T	T	Missense Variant	Allergic Disease (Asthma, Allergic Rhinitis)	-	29654163	FCER1B E237G polymorphism (rs569108) may serve as risk factor for allergic diseases.
25	FRMD6	rs3751464	C/T	C	Intron Variant	Exercise Induced Asthma	Hungarian (Caucasian) population	28293931	rs3751464 was associated with exercise-induced asthma.
26	FRMD6	rs9671722	A/C/G/T	G	Intron Variant	Exercise Induced Asthma	Hungarian (Caucasian) population	28293931	rs9671722 was associated with exercise-induced asthma.
27	FAM89A, TRIM67	rs12405429	C/T	T	Intergenic Variant	Asthma Remission	-	29786918	rs12405429 was associated with complete remission of asthma.
28	FLG-AS1	rs61816766	C/T	T	Intron Variant	Asthma, Allergic Diseases	European population	29785011	rs61816766 was associated with asthma and allergic diseases.
29	FOXP3	rs2280883	C/T	T	Intron Variant	Allergic Rhinitis	Chinese population	26791767	rs2280883 showed significant correlation with the efficacy of allergic rhinitis specific immune therapy.
30	FOXP3	rs2232365	A/G (REV)	A	Intron Variant	Allergic Rhinitis	Chinese population	26791767	rs2232365 showed significant correlation with the efficacy of allergic rhinitis specific immune therapy.
31	FOXP3	rs3761548	A/C/T (REV)	C	Intron Variant	Allergic Rhinitis	Chinese population	26791767	rs3761548 showed significant correlation with the efficacy of allergic rhinitis specific immune therapy.
32	FOXP3	rs3761549	C/T (REV)	C	Intron Variant	Allergic Rhinitis	Chinese population	26791767	rs3761549 showed significant correlation with the efficacy of allergic rhinitis specific immune therapy.
33	FOXP3	rs3761547	A/G (REV)	C	Intron Variant	Allergic Rhinitis	Chinese population	26791767	rs3761547 showed significant correlation with the efficacy of allergic rhinitis specific immune therapy.
34	FOXP3	rs17847095	G/T (REV)	G	Missense Variant	Allergic Rhinitis	Chinese population	26791767	rs17847095 showed significant correlation with the efficacy of allergic rhinitis specific immune therapy.
35	FLT4	rs10085109	C/G/T	G	Intron Variant	Atopic Dermatitis	Korean population	23490417	The rs10085109 SNP in the FLT4 gene were associated with susceptibility to Atopic Dermatitis.
36	FBXL7	rs10044254	A/G	A	Intron Variant	Childhood Asthma	-	24486069	rs10044254 was associated with both decreased expression of FBXL7 and improved symptomatic response to Inhaled Corticosteroids in 2 independent pediatric asthma cohorts.
37	FLG	rs11204981	A/G	A	2KB Upstream Variant	Asthma with Eczema	Iranian population	29569866	SNP in FLG (rs11204981) may serve as an important predictive marker for the combined eczema plus asthma phenotype, and that the highest level of expression in heterozygous may have a protective role in developing allergy phenotype.
38	FOXO3a	rs13217795	C/T	C	Intron Variant	Asthma	Indian population	26783460	An association between single nucleotide polymorphism of the FOXO3a (rs13217795, C>T transition) gene and asthma in Indian population was observed in this study.
39	FCER1B	rs1441586	C/T	C	Intron Variant	Childhood Asthma	Chinese Han population	19862939	FCER1B C-109T was significantly associated with childhood asthma.
40	FCER1B	rs569108	C/T	T	Missense Variant	Asthma	Chinese Han population	19862939	FCER1B E237G makes little contribution to the development of asthma in children of Chinese Han nationality.
41	FCER1B	rs1441586	C/T	C	Intron Variant	Aspirin-Intolerant Asthma (AIA)	Korean population	16839402	FcepsilonR1beta-109T > C polymorphism may increase expression of MS4A2 by mast cells, leading to enhanced release of proinflammatory mediators in the asthmatic airway, contributing to increased susceptibility to AIA.
42	FCER1G	-237A>G	A/G	-	-	Aspirin-Intolerant Asthma (AIA)	Korean population	18595682	The FCER1G-237A>G polymorphism may contribute to the development of AIA in a Korean population.
43	FCER1A	-344C>T	C/T	-	-	Aspirin-Intolerant Asthma (AIA)	Korean population	18595682	FCERIA-344C>T polymorphism may contribute to the development of AIA in a Korean population.