FADS1, fatty acid desaturase 1, 3992

N. diseases: 125; N. variants: 32
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs174547
rs174547
Entrez Id: 3992;9415
Gene Symbol: FADS1;FADS2
FADS1;FADS2
CUI: C1861172
Disease:
Venous Thromboembolism
0.010 GeneticVariation BEFREE In the secondary analysis, the minor allele of rs174547 in <i>FADS1</i> was associated with significantly lower odds of any ischemic stroke, large-artery stroke, and venous thromboembolism and showed suggestive evidence of inverse association with coronary artery disease, abdominal aortic aneurysm and aortic valve stenosis. 31817859 2019
dbSNP: rs174547
rs174547
Entrez Id: 3992;9415
Gene Symbol: FADS1;FADS2
FADS1;FADS2
CUI: C0948008
Disease:
Ischemic stroke
0.010 GeneticVariation BEFREE In the secondary analysis, the minor allele of rs174547 in <i>FADS1</i> was associated with significantly lower odds of any ischemic stroke, large-artery stroke, and venous thromboembolism and showed suggestive evidence of inverse association with coronary artery disease, abdominal aortic aneurysm and aortic valve stenosis. 31817859 2019
dbSNP: rs174547
rs174547
Entrez Id: 3992;9415
Gene Symbol: FADS1;FADS2
FADS1;FADS2
CUI: C0003507
Disease:
Aortic Valve Stenosis
0.010 GeneticVariation BEFREE In the secondary analysis, the minor allele of rs174547 in <i>FADS1</i> was associated with significantly lower odds of any ischemic stroke, large-artery stroke, and venous thromboembolism and showed suggestive evidence of inverse association with coronary artery disease, abdominal aortic aneurysm and aortic valve stenosis. 31817859 2019
dbSNP: rs174547
rs174547
Entrez Id: 3992;9415
Gene Symbol: FADS1;FADS2
FADS1;FADS2
CUI: C0010054
Disease:
Coronary Arteriosclerosis
0.010 GeneticVariation BEFREE In the secondary analysis, the minor allele of rs174547 in <i>FADS1</i> was associated with significantly lower odds of any ischemic stroke, large-artery stroke, and venous thromboembolism and showed suggestive evidence of inverse association with coronary artery disease, abdominal aortic aneurysm and aortic valve stenosis. 31817859 2019
dbSNP: rs174547
rs174547
Entrez Id: 3992;9415
Gene Symbol: FADS1;FADS2
FADS1;FADS2
CUI: C0007222
Disease:
Cardiovascular Diseases
0.010 GeneticVariation BEFREE We performed a secondary analysis of the association between a functional variant (rs174547) in <i>FADS1</i>, which encodes ?5-desaturase (a key enzyme in the endogenous FA synthesis), and CVD. 31817859 2019
dbSNP: rs3834458
rs3834458
Entrez Id: 3992;9415
Gene Symbol: FADS1;FADS2
FADS1;FADS2
CUI: C0400966
Disease:
Non-alcoholic Fatty Liver Disease
0.010 GeneticVariation BEFREE Serum FADS2 concentration was positively correlated with the susceptibility of NAFLD with CAD, while the polymorphism of rs3834458 was not associated with NAFLD with CAD. 31781193 2019
dbSNP: rs3834458
rs3834458
Entrez Id: 3992;9415
Gene Symbol: FADS1;FADS2
FADS1;FADS2
CUI: C1956346
Disease:
Coronary Artery Disease
0.010 GeneticVariation BEFREE Serum FADS2 concentration was positively correlated with the susceptibility of NAFLD with CAD, while the polymorphism of rs3834458 was not associated with NAFLD with CAD. 31781193 2019
dbSNP: rs3834458
rs3834458
Entrez Id: 3992;9415
Gene Symbol: FADS1;FADS2
FADS1;FADS2
CUI: C0010068
Disease:
Coronary heart disease
0.010 GeneticVariation BEFREE Association of Nonalcoholic Fatty Liver Disease and Coronary Artery Disease with FADS2 rs3834458 Gene Polymorphism in the Chinese Han Population. 31781193 2019
dbSNP: rs3834458
rs3834458
Entrez Id: 3992;9415
Gene Symbol: FADS1;FADS2
FADS1;FADS2
CUI: C0010054
Disease:
Coronary Arteriosclerosis
0.010 GeneticVariation BEFREE Association of Nonalcoholic Fatty Liver Disease and Coronary Artery Disease with FADS2 rs3834458 Gene Polymorphism in the Chinese Han Population. 31781193 2019
dbSNP: rs174546
rs174546
Entrez Id: 3992;9415
Gene Symbol: FADS1;FADS2
FADS1;FADS2
CUI: C0699791
Disease:
Stomach Carcinoma
0.010 GeneticVariation BEFREE In conclusion, we observed a significant inverse association between dietary DHA and the risk of gastric cancer but found that FADS1 rs174546 and FADS2 rs174583 did not modify the association between dietary n-3 or n-6 PUFAs and gastric cancer risk. 29491470 2018
dbSNP: rs174546
rs174546
Entrez Id: 3992;9415
Gene Symbol: FADS1;FADS2
FADS1;FADS2
CUI: C0024623
Disease:
Malignant neoplasm of stomach
0.010 GeneticVariation BEFREE In conclusion, we observed a significant inverse association between dietary DHA and the risk of gastric cancer but found that FADS1 rs174546 and FADS2 rs174583 did not modify the association between dietary n-3 or n-6 PUFAs and gastric cancer risk. 29491470 2018
dbSNP: rs174547
rs174547
Entrez Id: 3992;9415
Gene Symbol: FADS1;FADS2
FADS1;FADS2
CUI: C0242339
Disease:
Dyslipidemias
0.010 GeneticVariation BEFREE The results of this population-based study provide evidence for a relationship between lipid regulatory gene polymorphisms including GCKR (rs780094), GCKR (rs1260333), FADS (rs174547), and MLXIPL (rs3812316) with dyslipidemia in an Iranian population. 29858861 2018
dbSNP: rs174547
rs174547
Entrez Id: 3992;9415
Gene Symbol: FADS1;FADS2
FADS1;FADS2
CUI: C1269683
Disease:
Major Depressive Disorder
0.010 GeneticVariation BEFREE Minor alleles of rs174537 and rs174547 were significantly associated with lower odds of MDD (although significance was lost after correction for multiple comparisons). 28552045 2018
dbSNP: rs3834458
rs3834458
Entrez Id: 3992;9415
Gene Symbol: FADS1;FADS2
FADS1;FADS2
CUI: C1269683
Disease:
Major Depressive Disorder
0.010 GeneticVariation BEFREE Four erythrocyte long chain (LC) fatty acids (linoleic acid [LA], α-linolenic acid [ALA], arachidonic acid [AA] and Eicosapentaenoic acid [EPA]), as well as six SNPs (rs174537, rs174547, rs174570, rs174575, rs498793 and rs3834458) within the FADS gene cluster were measured in a sample of 207 participants (154 with MDD versus 53 non-depressed controls). 28552045 2018
dbSNP: rs968567
rs968567
Entrez Id: 3992;9415
Gene Symbol: FADS1;FADS2
FADS1;FADS2
CUI: C0010346
Disease:
Crohn Disease
0.010 GeneticVariation BEFREE These relate to SNPs associated with Crohn's disease (CD; rs102275) and rheumatoid arthritis (RA; rs968567), which affect the expression of miR-1908-5p (p<sub>rs102275</sub> = 1.44e-20, p<sub>rs968567</sub> = 2.54e-14). 30143393 2018
dbSNP: rs174548
rs174548
Entrez Id: 3992;9415
Gene Symbol: FADS1;FADS2
FADS1;FADS2
CUI: C1306460
Disease:
Primary malignant neoplasm of lung
0.010 GeneticVariation BEFREE Taken together, we found that rs174548 was associated with both PUFAs and lung cancer. 28968813 2017
dbSNP: rs174548
rs174548
Entrez Id: 3992;9415
Gene Symbol: FADS1;FADS2
FADS1;FADS2
CUI: C0684249
Disease:
Carcinoma of lung
0.010 GeneticVariation BEFREE Taken together, we found that rs174548 was associated with both PUFAs and lung cancer. 28968813 2017
dbSNP: rs174546
rs174546
Entrez Id: 3992;9415
Gene Symbol: FADS1;FADS2
FADS1;FADS2
CUI: C1956346
Disease:
Coronary Artery Disease
0.010 GeneticVariation BEFREE The present study suggests that the FADS1 rs174546 SNP and the FADS2 rs174601 SNP are associated with the risk of CAD and IS, and are likely to influence serum lipid levels. 26261632 2015
dbSNP: rs174546
rs174546
Entrez Id: 3992;9415
Gene Symbol: FADS1;FADS2
FADS1;FADS2
CUI: C0007222
Disease:
Cardiovascular Diseases
0.010 GeneticVariation BEFREE For the 11% of the population homozygous for the minor T-allele of rs174546 that associates with lower ∆5 FADS activity, high ALA intake and ALA-to-LA intake ratio may be preferable in the prevention of CVD and ischemic stroke. 25008580 2014
dbSNP: rs174556
rs174556
Entrez Id: 3992;9415
Gene Symbol: FADS1;FADS2
FADS1;FADS2
CUI: C0742343
Disease:
Acute Chest Syndrome
0.010 GeneticVariation BEFREE The trans-phase gene-gene interaction analysis showed that the combined genotype of rs174556 (T/T) and rs3756963 (T/T) was associated with ACS (P = 0.031). 23555103 2013
dbSNP: rs174556
rs174556
Entrez Id: 3992;9415
Gene Symbol: FADS1;FADS2
FADS1;FADS2
CUI: C0020538
Disease:
Hypertensive disease
0.010 GeneticVariation BEFREE And the results suggest that, for rs174556 C>T, the CT/TT genotypes were more likely to lead in ACS in subjects with hypertension after correction of all risk factors (OR = 4.236, 95% CI, 2.216-7.126). 23555103 2013
dbSNP: rs174547
rs174547
Entrez Id: 3992;9415
Gene Symbol: FADS1;FADS2
FADS1;FADS2
CUI: C0020473
Disease:
Hyperlipidemia
0.010 GeneticVariation BEFREE The CC variant of rs174547 was significantly associated with hyperlipidemia compared with the TT variant (adjusted odds ratio (OR)=1.71, 95% confidence intervals (CI): 1.16-2.54). 22490578 2012
dbSNP: rs174556
rs174556
Entrez Id: 3992;9415
Gene Symbol: FADS1;FADS2
FADS1;FADS2
CUI: C1956346
Disease:
Coronary Artery Disease
0.010 GeneticVariation BEFREE The trans phase gene-gene interaction analysis showed that the combined genotype of rs174556 (T/T) and rs3756963 (T/T) was weakly associated with the disease (P=0.043). rs174556 in the FADS1 gene is very likely to be associated with CAD in the Chinese Han population. 21917437 2011
dbSNP: rs174553
rs174553
Entrez Id: 3992;9415
Gene Symbol: FADS1;FADS2
FADS1;FADS2
CUI: C0432215
Disease:
Progressive pseudorheumatoid dysplasia
0.010 GeneticVariation BEFREE With haplotype ACCC (major alleles) for rs174553, rs99780, rs174575, rs174583, respectively, as reference, GTCT was positively associated with PPD risk at 36 weeks' gestation, p = 0.028, and higher LA and lower ARA in plasma (p = 0.0001, p < 0.0001) and RBC ethanolamine phospholipids (p = 0.007, p = 0.005). 20395685 2009
dbSNP: rs174547
rs174547
Entrez Id: 3992;9415
Gene Symbol: FADS1;FADS2
FADS1;FADS2
CUI: C0524620
Disease:
Metabolic Syndrome X
0.020 GeneticVariation BEFREE Korean carriers of the FADS1 rs174547 and FADS2 rs2845573 minor alleles have a greater susceptibility to MetS and moderate fat intake protected against the risk of MetS in carriers of the FADS1 major alleles. 29779171 2019