|
rs387906223
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
|
rs1801177
|
|
|
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 |
|
rs1217691063
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Hyperhomocysteinemia, serum folate levels and both C677T and A1298C MTHFR mutations are associated with CVD in HD patients.
|
12187094 |
2002 |
|
rs397507444
|
|
|
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
|
|
|
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 |
|
rs3135932
|
|
|
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 |
|
rs4986790
|
|
|
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 |
|
rs77375493
|
|
|
0.010 |
GeneticVariation |
BEFREE |
JAK2 V617F mutation is uncommon in non-Hodgkin lymphomas.
|
16321863 |
2006 |
|
rs4918
|
|
|
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
|
|
|
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
|
|
|
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 |
|
rs1801157
|
|
|
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 |
|
rs25487
|
|
|
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 |
|
rs759412116
|
|
|
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 |
|
rs1432295
|
|
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 |
|
rs1432295
|
|
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
|
|
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 |
|
rs2019960
|
|
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 |
|
rs2608053
|
|
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
|
|
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
|
|
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
|
|
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 |
|
rs6903608
|
|
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
|
|
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 |
|
rs4746
|
|
|
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 |