|
rs387906223
|
|
Hodgkin Disease
|
T |
0.700 |
CausalMutation
|
CLINVAR |
|
|
|
|
rs1801177
|
|
Hodgkin Disease
|
|
0.010 |
GeneticVariation
|
BEFREE |
Subjects with combined hyperlipidemia (CHL) were screened for mutations in the lipoprotein lipase (LPL) gene by single-strand conformational polymorphism, and a previously reported G-->A DNA sequence change in exon 2, causing substitution of Asp by Asn at position 9, was identified in 2 individuals.
|
7749858 |
1995 |
|
rs397507444
|
|
Hodgkin Disease
|
|
0.010 |
GeneticVariation
|
BEFREE |
Hyperhomocysteinemia, serum folate levels and both C677T and A1298C MTHFR mutations are associated with CVD in HD patients.
|
12187094 |
2002 |
|
rs1217691063
|
|
Hodgkin Disease
|
|
0.010 |
GeneticVariation
|
BEFREE |
Hyperhomocysteinemia, serum folate levels and both C677T and A1298C MTHFR mutations are associated with CVD in HD patients.
|
12187094 |
2002 |
|
rs1695
|
|
Hodgkin Disease
|
|
0.020 |
GeneticVariation
|
BEFREE |
The GSTP1 Ile(105)Val polymorphism was associated in a dose-dependent fashion with an improved failure-free survival in patients with Hodgkin's lymphoma (P = 0.02).
|
15788664 |
2005 |
|
rs77375493
|
|
Hodgkin Disease
|
|
0.010 |
GeneticVariation
|
BEFREE |
JAK2 V617F mutation is uncommon in non-Hodgkin lymphomas.
|
16321863 |
2006 |
|
rs4986790
|
|
Hodgkin Disease
|
|
0.010 |
GeneticVariation
|
BEFREE |
Furthermore, the TLR4 Asp299Gly variant was positively associated with the risk of mucosa-associated lymphoid tissue lymphoma (OR=2.76, 95% CI=1.12-6.81) and HL (OR=1.80, 95% CI=0.99-3.26).
|
16971956 |
2006 |
|
rs3135932
|
|
Hodgkin Disease
|
|
0.010 |
GeneticVariation
|
BEFREE |
The IL10RA Ser138Gly variant was underrepresented among lymphoma cases (odds ratio (OR)=0.81, 95 per cent confidence interval (95% CI)=0.65-1.02), mainly owing to an inverse association with Hodgkin's lymphoma (HL).
|
16971956 |
2006 |
|
rs4918
|
|
Hodgkin Disease
|
|
0.010 |
GeneticVariation
|
BEFREE |
In contrast with previous reports, this study suggests that CKD patients on HD treatment have a similar polymorphism distribution of the AHSG gene compared with the normal population and that the reduction in serum fetuin-A levels in Italian HD patients is not associated with an alteration in the distribution of AHSG T256S polymorphisms.
|
17851232 |
2007 |
|
rs4746
|
|
Hodgkin Disease
|
|
0.020 |
GeneticVariation
|
BEFREE |
Our aim was to study A419C (E111A) single nucleotide polymorphism (SNP) of the glyoxalase I gene in hemodialysis (HD) patients.
|
18079478 |
2008 |
|
rs397507545
|
|
Hodgkin Disease
|
|
0.010 |
GeneticVariation
|
BEFREE |
We describe the previously unreported condition of Hodgkin's lymphoma in a patient with Noonan syndrome caused by germ-line mutations (1507G > C, Gly503Arg) in exon 13 of the PTPN11 gene.
|
18758896 |
2008 |
|
rs759412116
|
|
Hodgkin Disease
|
|
0.010 |
GeneticVariation
|
BEFREE |
A positive association was found for XRCC1 gene polymorphism Arg399Gln (OR, 1.77; 95% confidence interval [95% CI], 1.16-2.71) and risk of HD.
|
19280628 |
2009 |
|
rs25487
|
|
Hodgkin Disease
|
|
0.010 |
GeneticVariation
|
BEFREE |
A positive association was found for XRCC1 gene polymorphism Arg399Gln (OR, 1.77; 95% confidence interval [95% CI], 1.16-2.71) and risk of HD.
|
19280628 |
2009 |
|
rs872071
|
|
Hodgkin Disease
|
|
0.010 |
GeneticVariation
|
BEFREE |
To examine if rs872071 genotype is associated with HL risk we genotyped two case-control series (totalling, 529 and 2192, respectively).
|
19804451 |
2010 |
|
rs1801157
|
|
Hodgkin Disease
|
|
0.010 |
GeneticVariation
|
BEFREE |
The single-nucleotide polymorphism (SNP) rs1801157 (previously known as CXCL12-A/ stromal cell-derived factor-1 (SDF1)-3'A) in CXCL12/SDF1 gene was assessed in breast cancer, Hodgkin's lymphoma (HL), and non-Hodgkin's lymphoma (NHL), since the chemokine CXCL12, previously known as SDF1, and its receptor CXCR4 regulate leukocyte trafficking and many essential biological processes, including tumor growth, angiogenesis, and metastasis of different types of tumors.
|
19927352 |
2009 |
|
rs4746
|
|
Hodgkin Disease
|
|
0.020 |
GeneticVariation
|
BEFREE |
The A419C (E111A) polymorphism of the GLO I gene is associated with vascular disease in hemodialysis (HD) patients and some RAGE gene polymorphisms are implicated in various pathological states.
|
20185929 |
2010 |
|
rs2070600
|
|
Hodgkin Disease
|
|
0.010 |
GeneticVariation
|
BEFREE |
To study the relationship of A419C GLO I and four RAGE polymorphisms (-429T/C, -374T/A, 2184A/G and Gly82Ser) in the prognosis of HD patients.
|
20185929 |
2010 |
|
rs1416580204
|
|
Hodgkin Disease
|
|
0.010 |
GeneticVariation
|
BEFREE |
To study the relationship of A419C GLO I and four RAGE polymorphisms (-429T/C, -374T/A, 2184A/G and Gly82Ser) in the prognosis of HD patients.
|
20185929 |
2010 |
|
rs6903608
|
|
Hodgkin Disease
|
G |
0.800 |
GeneticVariation
|
GWASDB |
A genome-wide association study of Hodgkin's lymphoma identifies new susceptibility loci at 2p16.1 (REL), 8q24.21 and 10p14 (GATA3).
|
21037568 |
2010 |
|
rs6903608
|
|
Hodgkin Disease
|
G |
0.800 |
GeneticVariation
|
GWASCAT |
A genome-wide association study of Hodgkin's lymphoma identifies new susceptibility loci at 2p16.1 (REL), 8q24.21 and 10p14 (GATA3).
|
21037568 |
2010 |
|
rs501764
|
|
Hodgkin Disease
|
C |
0.800 |
GeneticVariation
|
GWASCAT |
A genome-wide association study of Hodgkin's lymphoma identifies new susceptibility loci at 2p16.1 (REL), 8q24.21 and 10p14 (GATA3).
|
21037568 |
2010 |
|
rs501764
|
|
Hodgkin Disease
|
C |
0.800 |
GeneticVariation
|
GWASDB |
A genome-wide association study of Hodgkin's lymphoma identifies new susceptibility loci at 2p16.1 (REL), 8q24.21 and 10p14 (GATA3).
|
21037568 |
2010 |
|
rs2608053
|
|
Hodgkin Disease
|
G |
0.800 |
GeneticVariation
|
GWASDB |
A genome-wide association study of Hodgkin's lymphoma identifies new susceptibility loci at 2p16.1 (REL), 8q24.21 and 10p14 (GATA3).
|
21037568 |
2010 |
|
rs2608053
|
|
Hodgkin Disease
|
G |
0.800 |
GeneticVariation
|
GWASCAT |
A genome-wide association study of Hodgkin's lymphoma identifies new susceptibility loci at 2p16.1 (REL), 8q24.21 and 10p14 (GATA3).
|
21037568 |
2010 |
|
rs2019960
|
|
Hodgkin Disease
|
G |
0.800 |
GeneticVariation
|
GWASDB |
A genome-wide association study of Hodgkin's lymphoma identifies new susceptibility loci at 2p16.1 (REL), 8q24.21 and 10p14 (GATA3).
|
21037568 |
2010 |