Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10741657
rs10741657
Entrez Id: 120227
Gene Symbol: CYP2R1
CYP2R1
CUI: C0042870
Disease:
Vitamin D Deficiency
0.820 GeneticVariation BEFREE Published articles provide evidence supporting a major role for the rs10741657 polymorphism of the CYP2R1 gene in determining 25(OH)D levels and the presence of vitamin D deficiency. 30120973 2018
dbSNP: rs10741657
rs10741657
Entrez Id: 120227
Gene Symbol: CYP2R1
CYP2R1
CUI: C0042870
Disease:
Vitamin D Deficiency
0.820 GeneticVariation BEFREE The presence of GG allele of the SNP rs2228570 of VDR gene, SNPs rs4588 of GC gene and CYP2R1 rs10741657 gene was associated with vitamin D deficiency. 27570856 2016
dbSNP: rs10741657
rs10741657
Entrez Id: 120227
Gene Symbol: CYP2R1
CYP2R1
CUI: C0042870
Disease:
Vitamin D Deficiency
0.820 GeneticVariation GWASDB Common genetic determinants of vitamin D insufficiency: a genome-wide association study. 20541252 2010
dbSNP: rs10741657
rs10741657
Entrez Id: 120227
Gene Symbol: CYP2R1
CYP2R1
CUI: C0042870
Disease:
Vitamin D Deficiency
0.820 GeneticVariation GWASCAT Common genetic determinants of vitamin D insufficiency: a genome-wide association study. 20541252 2010
dbSNP: rs2060793
rs2060793
Entrez Id: 120227
Gene Symbol: CYP2R1
CYP2R1
CUI: C0919758
Disease:
Vitamin D measurement
A 0.800 GeneticVariation GWASCAT Suggestive signals for association with 25(OH)D were also observed for SNPs in or near three other genes involved in vitamin D synthesis or activation: rs3829251 on chromosome 11q13.4 in NADSYN1 [encoding nicotinamide adenine dinucleotide (NAD) synthetase; P=8.8x10(-7)], which was in high LD with rs1790349, located in DHCR7, the gene encoding 7-dehydrocholesterol reductase that synthesizes cholesterol from 7-dehydrocholesterol; rs6599638 in the region harboring the open-reading frame 88 (C10orf88) on chromosome 10q26.13 in the vicinity of ACADSB (acyl-Coenzyme A dehydrogenase), involved in cholesterol and vitamin D synthesis (P=3.3x10(-7)); and rs2060793 on chromosome 11p15.2 in CYP2R1 (cytochrome P450, family 2, subfamily R, polypeptide 1, encoding a key C-25 hydroxylase that converts vitamin D3 to an active vitamin D receptor ligand; P=1.4x10(-5)). 20418485 2010
dbSNP: rs2060793
rs2060793
Entrez Id: 120227
Gene Symbol: CYP2R1
CYP2R1
CUI: C0523979
Disease:
Vitamin D3 measurement
A 0.800 GeneticVariation GWASDB Suggestive signals for association with 25(OH)D were also observed for SNPs in or near three other genes involved in vitamin D synthesis or activation: rs3829251 on chromosome 11q13.4 in NADSYN1 [encoding nicotinamide adenine dinucleotide (NAD) synthetase; P=8.8x10(-7)], which was in high LD with rs1790349, located in DHCR7, the gene encoding 7-dehydrocholesterol reductase that synthesizes cholesterol from 7-dehydrocholesterol; rs6599638 in the region harboring the open-reading frame 88 (C10orf88) on chromosome 10q26.13 in the vicinity of ACADSB (acyl-Coenzyme A dehydrogenase), involved in cholesterol and vitamin D synthesis (P=3.3x10(-7)); and rs2060793 on chromosome 11p15.2 in CYP2R1 (cytochrome P450, family 2, subfamily R, polypeptide 1, encoding a key C-25 hydroxylase that converts vitamin D3 to an active vitamin D receptor ligand; P=1.4x10(-5)). 20418485 2010
dbSNP: rs2060793
rs2060793
Entrez Id: 120227
Gene Symbol: CYP2R1
CYP2R1
CUI: C0919758
Disease:
Vitamin D measurement
A 0.800 GeneticVariation GWASDB Suggestive signals for association with 25(OH)D were also observed for SNPs in or near three other genes involved in vitamin D synthesis or activation: rs3829251 on chromosome 11q13.4 in NADSYN1 [encoding nicotinamide adenine dinucleotide (NAD) synthetase; P=8.8x10(-7)], which was in high LD with rs1790349, located in DHCR7, the gene encoding 7-dehydrocholesterol reductase that synthesizes cholesterol from 7-dehydrocholesterol; rs6599638 in the region harboring the open-reading frame 88 (C10orf88) on chromosome 10q26.13 in the vicinity of ACADSB (acyl-Coenzyme A dehydrogenase), involved in cholesterol and vitamin D synthesis (P=3.3x10(-7)); and rs2060793 on chromosome 11p15.2 in CYP2R1 (cytochrome P450, family 2, subfamily R, polypeptide 1, encoding a key C-25 hydroxylase that converts vitamin D3 to an active vitamin D receptor ligand; P=1.4x10(-5)). 20418485 2010
dbSNP: rs2060793
rs2060793
Entrez Id: 120227
Gene Symbol: CYP2R1
CYP2R1
CUI: C0523979
Disease:
Vitamin D3 measurement
A 0.800 GeneticVariation GWASCAT Suggestive signals for association with 25(OH)D were also observed for SNPs in or near three other genes involved in vitamin D synthesis or activation: rs3829251 on chromosome 11q13.4 in NADSYN1 [encoding nicotinamide adenine dinucleotide (NAD) synthetase; P=8.8x10(-7)], which was in high LD with rs1790349, located in DHCR7, the gene encoding 7-dehydrocholesterol reductase that synthesizes cholesterol from 7-dehydrocholesterol; rs6599638 in the region harboring the open-reading frame 88 (C10orf88) on chromosome 10q26.13 in the vicinity of ACADSB (acyl-Coenzyme A dehydrogenase), involved in cholesterol and vitamin D synthesis (P=3.3x10(-7)); and rs2060793 on chromosome 11p15.2 in CYP2R1 (cytochrome P450, family 2, subfamily R, polypeptide 1, encoding a key C-25 hydroxylase that converts vitamin D3 to an active vitamin D receptor ligand; P=1.4x10(-5)). 20418485 2010
dbSNP: rs61495246
rs61495246
Entrez Id: 120227
Gene Symbol: CYP2R1
CYP2R1
CUI: C1838657
Disease:
Vitamin D Hydroxylation-Deficient Rickets, Type 1B
G 0.800 CausalMutation CLINVAR
dbSNP: rs61495246
rs61495246
Entrez Id: 120227
Gene Symbol: CYP2R1
CYP2R1
CUI: C1838657
Disease:
Vitamin D Hydroxylation-Deficient Rickets, Type 1B
0.800 GeneticVariation UNIPROT
dbSNP: rs10741657
rs10741657
Entrez Id: 120227
Gene Symbol: CYP2R1
CYP2R1
CUI: C0919758
Disease:
Vitamin D measurement
A 0.700 GeneticVariation GWASCAT Genome-wide association study in 79,366 European-ancestry individuals informs the genetic architecture of 25-hydroxyvitamin D levels. 29343764 2018
dbSNP: rs10741657
rs10741657
Entrez Id: 120227
Gene Symbol: CYP2R1
CYP2R1
CUI: C0523979
Disease:
Vitamin D3 measurement
A 0.700 GeneticVariation GWASCAT Genome-wide association study in 79,366 European-ancestry individuals informs the genetic architecture of 25-hydroxyvitamin D levels. 29343764 2018
dbSNP: rs117913124
rs117913124
Entrez Id: 120227
Gene Symbol: CYP2R1
CYP2R1
CUI: C0919758
Disease:
Vitamin D measurement
A 0.700 GeneticVariation GWASCAT Genome-Wide Association Study of Serum 25-Hydroxyvitamin D in US Women. 29545823 2018
dbSNP: rs117913124
rs117913124
Entrez Id: 120227
Gene Symbol: CYP2R1
CYP2R1
CUI: C0523979
Disease:
Vitamin D3 measurement
A 0.700 GeneticVariation GWASCAT Genome-Wide Association Study of Serum 25-Hydroxyvitamin D in US Women. 29545823 2018
dbSNP: rs1993116
rs1993116
Entrez Id: 120227
Gene Symbol: CYP2R1
CYP2R1
CUI: C0523979
Disease:
Vitamin D3 measurement
0.700 GeneticVariation GWASDB Genome-wide association study of circulating vitamin D levels. 20418485 2010
dbSNP: rs1993116
rs1993116
Entrez Id: 120227
Gene Symbol: CYP2R1
CYP2R1
CUI: C0919758
Disease:
Vitamin D measurement
0.700 GeneticVariation GWASDB Genome-wide association study of circulating vitamin D levels. 20418485 2010
dbSNP: rs10741657
rs10741657
Entrez Id: 120227
Gene Symbol: CYP2R1
CYP2R1
CUI: C0019196
Disease:
Hepatitis C
0.020 GeneticVariation BEFREE The results showed that the CYP2R1 rs12794714-G, rs10741657-A, rs1562902-C, and rs10766197-G alleles were significantly associated with increased susceptibility to HCV infection (all P<sub>FDR</sub> < 0.05, in additive/dominant models), and the combined effect of the four unfavorable alleles was related to an elevated risk of HCV infection in a locus-dosage manner (P<sub>trend</sub> = 0.008). 31520221 2019
dbSNP: rs12794714
rs12794714
Entrez Id: 120227
Gene Symbol: CYP2R1
CYP2R1
CUI: C0011854
Disease:
Diabetes Mellitus, Insulin-Dependent
0.020 GeneticVariation BEFREE CYP2R1 rs12794714 and rs10766196 polymorphisms were associated with a higher risk of type 1 diabetes. 31206955 2019
dbSNP: rs10741657
rs10741657
Entrez Id: 120227
Gene Symbol: CYP2R1
CYP2R1
CUI: C0010054
Disease:
Coronary Arteriosclerosis
0.020 GeneticVariation BEFREE Two 25(OH)D reducing genetic variants in the DCHR7 gene (rs7944926 and rs11234027) and two in the CYP2R1 gene (rs10741657 and rs12794714) were genotyped in 92 416 participants of Danish descent, of whom 14 455 developed ischaemic heart disease (ICD-8:410-414; ICD-10:I20-I25) and 7061 myocardial infarction (ICD-8:410: ICD-10:I21-I22) from 1977 through 2011. 25981321 2015
dbSNP: rs12794714
rs12794714
Entrez Id: 120227
Gene Symbol: CYP2R1
CYP2R1
CUI: C0010054
Disease:
Coronary Arteriosclerosis
0.020 GeneticVariation BEFREE Two 25(OH)D reducing genetic variants in the DCHR7 gene (rs7944926 and rs11234027) and two in the CYP2R1 gene (rs10741657 and rs12794714) were genotyped in 92 416 participants of Danish descent, of whom 14 455 developed ischaemic heart disease (ICD-8:410-414; ICD-10:I20-I25) and 7061 myocardial infarction (ICD-8:410: ICD-10:I21-I22) from 1977 through 2011. 25981321 2015
dbSNP: rs10741657
rs10741657
Entrez Id: 120227
Gene Symbol: CYP2R1
CYP2R1
CUI: C0010054
Disease:
Coronary Arteriosclerosis
0.020 GeneticVariation BEFREE Triangular relationship between single nucleotide polymorphisms in the CYP2R1 gene (rs10741657 and rs12794714), 25-hydroxyvitamin d levels, and coronary artery disease incidence. 25003556 2014
dbSNP: rs12794714
rs12794714
Entrez Id: 120227
Gene Symbol: CYP2R1
CYP2R1
CUI: C0009402
Disease:
Colorectal Carcinoma
0.020 GeneticVariation BEFREE In this study, no significant difference was observed for VDR (rs2238136), GC (rs4588), CYP2R1 (rs12794714), and CYP27B1 (rs3782130) gene variants in either genotype or allele frequencies between the cases with CRC and the controls and this lack of difference remained even after adjustment for age, BMI, sex, smoking status, NSAID use, and family history of CRC. 24568525 2014
dbSNP: rs12794714
rs12794714
Entrez Id: 120227
Gene Symbol: CYP2R1
CYP2R1
CUI: C0009402
Disease:
Colorectal Carcinoma
0.020 GeneticVariation BEFREE A nominally significant association was detected between CRC and the SNP rs12794714 in the vitamin D 25-hydroxylase gene CYP2R1 (p = 0.019), a SNP that has previously been associated with serum vitamin D levels. 24562971 2014
dbSNP: rs12794714
rs12794714
Entrez Id: 120227
Gene Symbol: CYP2R1
CYP2R1
CUI: C0010054
Disease:
Coronary Arteriosclerosis
0.020 GeneticVariation BEFREE Triangular relationship between single nucleotide polymorphisms in the CYP2R1 gene (rs10741657 and rs12794714), 25-hydroxyvitamin d levels, and coronary artery disease incidence. 25003556 2014
dbSNP: rs10741657
rs10741657
Entrez Id: 120227
Gene Symbol: CYP2R1
CYP2R1
CUI: C0019196
Disease:
Hepatitis C
0.020 GeneticVariation BEFREE The well-known associations between CYP2R1 (rs1993116, rs10741657), GC (rs2282679), and DHCR7 (rs7944926, rs12785878) genotypes and 25(OH)D3 serum levels were also apparent in patients with chronic hepatitis C. The same genotypes of these single nucleotide polymorphisms (SNPs) that are associated with reduced 25(OH)D3 serum levels were found to be associated with HCV-related HCC (P = 0.07 [OR = 1.13, 95% CI = 0.99-1.28] for CYP2R1, P = 0.007 [OR = 1.56, 95% CI = 1.12-2.15] for GC, P = 0.003 [OR = 1.42, 95% CI = 1.13-1.78] for DHCR7; ORs for risk genotypes). 23734184 2013