Browse Result

Total number of records for in V of in DAAB (Version-2) database: 29

 

Record noGENE NAMESNP IDCHANGESANCESTRAL ALLELESFUNCTIONAL CONSEQUENCESDISEASEPOPULATIONPubmed IDComments
1VDBPrs7041A/G/TTMissense VariantBronchial Asthma (In Children and Adolescents)Egyptian Population30548492rs7041 GG genotype and G allele increased asthma risk. The control group has a higher carriage rate of T allele.
2VDBPrs4588A/C/TCMissense VariantBronchial Asthma (In Children and Adolescents)Egyptian Population30548492rs4588 AA genotype and A allele conferred protection in the Egyptian population. The carriage rate of C allele is higher among asthma patients.
3VEGFrs3025020C/TCIntron VariantAsthmaChinese Han population27173321 The T allele in rs3025020 was significantly more prevalent in the asthma group than in controls. The VEGF SNPs rs3025020 may be associated with the development of asthma, indicating the role of VEGF in asthma.
4VEGFrs3025039 C/TC3 Prime UTR VariantAsthmaChinese Han population27173321 The T allele in rs3025039 was significantly more prevalent in the asthma group than in controls. The VEGF SNPs rs3025039 may be associated with the development of asthma, indicating the role of VEGF in asthma.
5VDRrs7975232A/CCIntron VariantChildhood AsthmaAsian population, Non Asian population27551963The risk of developing childhood asthma was almost 1.5-fold higher in Asians with ApaI (rs7975232) G allele.
6VDRrs1544410A/C/G/TGIntron VariantChildhood Asthma-27551963BsmI (rs1544410) polymorphism marginally contributes to childhood asthma susceptibility.
7VDRrs2228570A/C/G/TTInitiator Codon VariantChildhood AsthmaCaucasian population27551963The FokI (rs2228570) G allele may increase the asthma risk compared with the A allele in Caucasian population.
8VDRrs4328262A/G/TTIntron VariantViral Respiratory Illness, AsthmaEuropean or American European26399222rs4328262 was significantly associated with variation in eight of the 10 RhinoGen phenotypes and with asthma at age 6 in the COAST (Childhood Origins of Asthma) study. Specifically, the TT genotype at rs4328262 was associated with fewer observed illnesses, decreased cold symptom burden, and less loss of asthma control in children in RhinoGen, and with less asthma at age 6 years in the COAST children.
9VDRrs2228570A/C/G/TTInitiator Codon VariantChildhood Bronchial AsthmaChinese Han ethnicity28590769Significant associations was found between rs2228570 of VDR and susceptibility to and prognosis of childhood bronchial asthma, providing novel target for treating the disorder.
10VDRrs7975232A/CCIntron VariantChildhood Bronchial AsthmaChinese Han ethnicity28590769Significant associations was found between rs7975232 of VDR and susceptibility to and prognosis of childhood bronchial asthma, providing novel target for treating the disorder. The haplotype analysis suggested that CA rs7975232 was correlated with levels of VD, IL-4, and IL-5.
11VDRrs1544410 A/C/G/TGIntron VariantChildhood Bronchial AsthmaChinese Han ethnicity28590769Significant associations was found between rs1544410 of VDR and susceptibility to and prognosis of childhood bronchial asthma, providing novel target for treating the disorder. The haplotype analysis suggested that AG rs1544410 was correlated with levels of VD, IL-4, and IL-5.
12VDR rs2228570 A/C/G/T(REV)TInitiator Codon VariantAsthma-27088875rs2228570 gene polymorphism in VDR is associated with increased susceptibility to asthma, indicating VDR polymorphism could be developed as biomarker for asthma susceptibility.
13VDR rs7975232A/CCIntron VariantAsthma-27088875rs7975232 gene polymorphism in VDR are associated with increased susceptibility to asthma, indicating VDR polymorphism could be developed as biomarker for asthma susceptibility.
14VDR rs731236 C/T (REV)TSynonymous VariantAsthma-27088875rs731236 gene polymorphism in VDR are associated with increased susceptibility to asthma, indicating VDR polymorphism could be developed as biomarker for asthma susceptibility.
15VDR rs3782905 C/G (REV)CIntron VariantAsthma-27088875rs3782905 gene polymorphism in VDR are associated with increased susceptibility to asthma, indicating VDR polymorphism could be developed as biomarker for asthma susceptibility.
16VDRrs7975232 A/CCIntron VariantChildhood Bronchial AsthmaChinese population29456680The locus CC frequency of rs7975232 of VDR gene in observation group was lower in the asthma group than that in the control group; the locus AC and AA frequencies of rs7975232 of VDR gene were higher in the asthma group than those in the control group.
17VDRrs2228570A/C/G/T (REV)TInitiator Codon VariantBronchial AsthmaSerbian population28407346FF genotype and F allele of FokI SNP (rs2228570) of VDR exerts a protective role on Bronchial Asthma development in Serbian population.
18VEGFrs2010963C/GG5 Prime UTR VariantAsthmaTunisian population19787077A borderline association with asthma was found for the G allele in the −634G > C polymorphism (rs2010963).
19VEGFrs2146323A/CCIntron VariantAsthmaSlovenian population22519966Polymorphism rs2146323 A>C in VEGFA was associated with response to Inhaled Corticosteroid therapy in asthmatics. Asthma patients with the AA genotype had a greater improvement in the %predicted FEV(1) than those with the AC or CC genotype. Conversely, the AA genotype in rs2146323 was associated with uncontrolled asthma in patients regularly receiving LTRA therapy and a worse FEV(1)/FVC ratio in asthma patients who episodically used LTRA therapy.
20VEGFrs833058C/TT-AsthmaSlovenian population22519966Polymorphism rs833058 C>T was associated with treatment response to episodically used LTRA therapy in asthmatics. A subgroup of asthma patients with the TT genotype had an improvement in the %predicted FEV(1) as compared with no improvement in patients with the CT or CC genotype.
21VEGF-2549 -2567 del18 --DeletionAsthmaPolish population30574871The presence of del18 genotype at -2549 -2567 position in the promoter of VEGF gene along with disease duration and other factors like cigarette smoking, associate with the risk of irreversible bronchoconstriction in asthmatics.
22VEGFrs1479430148A/T-3 Prime UTR VariantAllergic RhinitisMalaysian Chinese population30215845AA genotype in rs1479430148 (VEGFA) was significantly associated with allergic rhinitis in mixed (pigmented-vascular) subtype.
23VEGFArs2010963C/GG5 Prime UTR VariantAtopic DermatitisKorean population23490417The rs2010963 SNP had a marginally significant effect on log-eosinophil counts in atopic dermatitis patients.
24VDRrs2228570A/C/G/TTInitiator Codon VariantAsthmaAustralian population32380236Children with rs2228570 AA genotype had higher exacerbation severity scores (p=0.001) and poorer β2-agonist treatment response.
25VDRrs1544410A/C/G/TGIntron VariantAsthmaAustralian population32380236Children with rs1544410 (BsmI) TT genotype had lower exacerbation severity scores as compared to those with the CC genotype.
26VDRrs739837C/G/TT3 Prime UTR VariantAsthmaChinese population32157950The minor allele (T) of rs739837 significantly increased the severity of asthma.
27VDRrs7975232A/CCIntron VariantAllergic RhinitisChinese population31163545The polymorphism of ApaⅠ(rs7975232) locus of VDR gene is correlated with Allergic Rhinitis susceptibility.
28VDRrs731236C/T (REV)TSynonymous VariantAsthmaIrish population29384117TaqI polymorphism was associated with asthma in Irish children.
29VDRrs7975232A/CCIntron VariantAsthmaIrish population29384117ApaI polymorphism was associated with asthma in Irish children.