Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs731236
rs731236
VDR
CUI: C0023343
Disease: Leprosy
Leprosy
0.010 GeneticVariation BEFREE Some polymorphisms of the <i>VDR</i> gene, such as <i>Bsm</i>I (G>A rs1544410)<i>, Apa</i>I (G>T rs7975232), and <i>Taq</i>I (T>C rs731236) could affect its stability and mRNA transcription activity, while <i>Fok</i>I T>C (rs2228570) gives a truncated protein with three fewer amino acids and more efficiency in binding vitamin D. This study evaluated these four polymorphisms in the immunopathogenesis of leprosy in 404 patients and 432 control individuals without chronic or infectious disease in southern Brazil. 31636627

2019

dbSNP: rs731236
rs731236
VDR
CUI: C0029453
Disease: Osteopenia
Osteopenia
0.010 GeneticVariation BEFREE The presence of the TT allele of the SNP rs2228570 of the VDR gene and the SNP rs731236 of the CC genotype was associated with the presence of osteopenia and decreased bone mineral density alongside malfunctions of vitamin D. 30963970

2019

dbSNP: rs731236
rs731236
VDR
CUI: C0221775
Disease: Lumbar disc disease
Lumbar disc disease
0.010 GeneticVariation BEFREE TaqI (rs731236) polymorphism was associated with a predisposition to LDD. 31127184

2019

dbSNP: rs731236
rs731236
VDR
CUI: C0003864
Disease: Arthritis
Arthritis
0.010 GeneticVariation BEFREE The rs10735810, rs1544410, rs7975232, and rs731236 were associated with the onset of arthritis at both allelic and genotypic level (p < 0.01). 31011579

2019

dbSNP: rs731236
rs731236
VDR
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.010 GeneticVariation BEFREE Our results indicate that VDR rs731236 & rs2228570 or VDBP rs7041 polymorphisms were not risk factors for the development of gastric cancer individually, however, lower serum levels of vitamin D may be a contributory risk for both predisposition and development of gastric cancer. 31549372

2019

dbSNP: rs731236
rs731236
VDR
CUI: C0029456
Disease: Osteoporosis
Osteoporosis
0.010 GeneticVariation BEFREE In this study, VDR gene <i>ApaI</i> (rs7975232), <i>BsmI</i> (rs 1544410) and <i>TaqI</i> (rs731236) genotypes were compared in men with osteoporosis and male controls. 31448632

2019

dbSNP: rs731236
rs731236
VDR
CUI: C0266929
Disease: Chronic Periodontitis
Chronic Periodontitis
0.010 GeneticVariation BEFREE There was no significant association between genotype/phenotype of VDBP's SNPs (rs7041 and rs4588) and occurrence of chronic periodontitis (p value = 0.401) Moreover, no statistically significant association was found between chronic periodontitis and Taq1 (rs731236) (p value = 0.401) and Apa1 (rs7975232) (p value = 0.248). 30083974

2019

dbSNP: rs731236
rs731236
VDR
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.010 GeneticVariation BEFREE Our results indicate that VDR rs731236 & rs2228570 or VDBP rs7041 polymorphisms were not risk factors for the development of gastric cancer individually, however, lower serum levels of vitamin D may be a contributory risk for both predisposition and development of gastric cancer. 31549372

2019

dbSNP: rs731236
rs731236
VDR
CUI: C0041327
Disease: Tuberculosis, Pulmonary
Tuberculosis, Pulmonary
0.010 GeneticVariation BEFREE Vitamin D receptor ApaI (rs7975232), BsmI (rs1544410), Fok1 (rs2228570), and TaqI (rs731236) gene polymorphisms and susceptibility to pulmonary tuberculosis in an Iranian population: A systematic review and meta-analysis. 31740220

2019

dbSNP: rs731236
rs731236
VDR
CUI: C0040021
Disease: Thromboangiitis Obliterans
Thromboangiitis Obliterans
0.010 GeneticVariation BEFREE The study aimed to evaluate the association of selected <i>VDR</i> polymorphisms (rs2228570, rs1544410, rs7975232, rs731236, and rs11568820) with susceptibility to TAO. 31424978

2019

dbSNP: rs731236
rs731236
VDR
CUI: C0391826
Disease: Lhermitte-Duclos disease
Lhermitte-Duclos disease
0.010 GeneticVariation BEFREE TaqI (rs731236) polymorphism was associated with a predisposition to LDD. 31127184

2019

dbSNP: rs731236
rs731236
VDR
CUI: C0026848
Disease: Myopathy
Myopathy
0.010 GeneticVariation BEFREE The CC-genotype of the VDR polymorphism TaqI rs731236 has previously been associated with a higher risk of developing myopathy compared to TT-carriers. 31252402

2019

dbSNP: rs731236
rs731236
VDR
CUI: C0033860
Disease: Psoriasis
Psoriasis
0.010 GeneticVariation BEFREE The currently available data fails to support a robust association between VDR rs7975232, rs1544410, rs2228570 and rs731236 polymorphisms and psoriasis susceptibility, which still required the support of more case-control studies. 31623568

2019

dbSNP: rs731236
rs731236
VDR
CUI: C0007134
Disease: Renal Cell Carcinoma
Renal Cell Carcinoma
0.010 GeneticVariation BEFREE This meta-analysis was conducted to assess the association of VDR ApaI (rs7975232), BsmI (rs1544410), TaqI (rs731236), and Fok1 (rs2228570) gene polymorphisms with RCC risk. 29970659

2018

dbSNP: rs731236
rs731236
VDR
CUI: C0029458
Disease: Osteoporosis, Postmenopausal
Osteoporosis, Postmenopausal
0.010 GeneticVariation BEFREE For the bearers of C-G-C haplotype (consisting of rs7975232, rs1544410, and rs731236 unfavorable alleles), the risk of PMO was significantly higher (OR = 4.7, 95% CI 2.8-8.1, <i>p</i> < 0.0001) compared to controls. 29922235

2018

dbSNP: rs731236
rs731236
VDR
CUI: C3840565
Disease: Autoimmune thyroid disease (AITD)
Autoimmune thyroid disease (AITD)
0.010 GeneticVariation BEFREE The overall results indicated that <i>VDR</i> rs731236 and rs2228570 polymorphisms were significantly associated with a reduced risk of AITD. 29765404

2018

dbSNP: rs731236
rs731236
VDR
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.010 GeneticVariation BEFREE The synonymous single nucleotide polymorphism (SNP) rs731236, located in the VDR gene, has been associated with a higher risk of Crohn's disease (CD). 29788141

2018

dbSNP: rs731236
rs731236
VDR
CUI: C0029408
Disease: Degenerative polyarthritis
Degenerative polyarthritis
0.010 GeneticVariation BEFREE The rs731236 polymorphism is associated with the risk of primary OA of the knee in Mexican Mestizo population. 30657057

2018

dbSNP: rs731236
rs731236
VDR
CUI: C0456103
Disease: Sepsis of the newborn
Sepsis of the newborn
0.010 GeneticVariation BEFREE We aimed to investigate the association of VDR polymorphism at FokI, rs2228570 T/C, and TaqI, rs731236 C/T gene with serum 25-hydroxyvitamin D level and risk of neonatal sepsis. 29530503

2018

dbSNP: rs731236
rs731236
VDR
CUI: C0020443
Disease: Hypercholesterolemia
Hypercholesterolemia
0.010 GeneticVariation BEFREE The rs731236 variant was shown to be associated with high cholesterol and LDL-cholesterol levels in T2DM patients, while rs1544410 was associated with lower BMI and lower LDL cholesterol levels. 28323045

2018

dbSNP: rs731236
rs731236
VDR
CUI: C0003855
Disease: Arteriovenous fistula
Arteriovenous fistula
0.010 GeneticVariation BEFREE We investigated the influence of the vitamin D receptor gene TaqI (rs731236), ApaI (rs7975232), and FokI (rs2228570) polymorphisms in arteriovenous fistula failure in hemodialysis patients. 29544394

2018

dbSNP: rs731236
rs731236
VDR
Conventional (Clear Cell) Renal Cell Carcinoma
0.010 GeneticVariation BEFREE This meta-analysis was conducted to assess the association of VDR ApaI (rs7975232), BsmI (rs1544410), TaqI (rs731236), and Fok1 (rs2228570) gene polymorphisms with RCC risk. 29970659

2018

dbSNP: rs731236
rs731236
VDR
CUI: C3665339
Disease: Bacterial sepsis of newborn
Bacterial sepsis of newborn
0.010 GeneticVariation BEFREE We aimed to investigate the association of VDR polymorphism at FokI, rs2228570 T/C, and TaqI, rs731236 C/T gene with serum 25-hydroxyvitamin D level and risk of neonatal sepsis. 29530503

2018

dbSNP: rs731236
rs731236
VDR
CUI: C0566602
Disease: Primary sclerosing cholangitis
Primary sclerosing cholangitis
0.010 GeneticVariation BEFREE We investigated the incidence of VDR polymorphisms (rs1544410-BsmI; rs7975232-ApaI; rs731236-TaqI) in a group of patients with primary sclerosing cholangitis (PSC, n = 275) and in healthy controls (n = 376). 28426778

2017

dbSNP: rs731236
rs731236
VDR
CUI: C0001430
Disease: Adenoma
Adenoma
0.010 GeneticVariation BEFREE The effect of vitamin D3 supplementation on advanced adenomas, but not on adenoma risk overall, significantly varied according to genotype at 2 VDR SNPs (rs7968585 and rs731236) in linkage disequilibrium (D' = 0.98; r2 = 0.6). 27978548

2017