rs1052501
|
|
|
0.810 |
GeneticVariation |
BEFREE |
Common single-nucleotide polymorphisms (SNPs) at 2p23.3 (rs6746082), 3p22.1 (rs1052501), 3q26.2 (rs10936599), 6p21.33 (rs2285803), 7p15.3 (rs4487645), 17p11.2 (rs4273077), and 22q13.1 (rs877529) have recently been shown to influence MM risk.
|
24449210 |
2014 |
rs1052501
|
|
G |
0.810 |
GeneticVariation |
GWASDB |
Common variation at 3q26.2, 6p21.33, 17p11.2 and 22q13.1 influences multiple myeloma risk.
|
23955597 |
2013 |
rs1052501
|
|
G |
0.810 |
GeneticVariation |
GWASCAT |
We identified risk loci for multiple myeloma at 3p22.1 (rs1052501 in ULK4; odds ratio (OR) = 1.32; P = 7.47 × 10(-9)) and 7p15.3 (rs4487645, OR = 1.38; P = 3.33 × 10(-15)).
|
22120009 |
2011 |
rs1052501
|
|
G |
0.810 |
GeneticVariation |
GWASDB |
We identified risk loci for multiple myeloma at 3p22.1 (rs1052501 in ULK4; odds ratio (OR) = 1.32; P = 7.47 × 10(-9)) and 7p15.3 (rs4487645, OR = 1.38; P = 3.33 × 10(-15)).
|
22120009 |
2011 |
rs6763508
|
|
C |
0.800 |
GeneticVariation |
GWASCAT |
Genome-wide association analysis of chronic lymphocytic leukaemia, Hodgkin lymphoma and multiple myeloma identifies pleiotropic risk loci.
|
28112199 |
2017 |
rs6599192
|
|
G |
0.800 |
GeneticVariation |
GWASCAT |
Genome-wide association study identifies multiple susceptibility loci for multiple myeloma.
|
27363682 |
2016 |
rs73071352
|
|
G |
0.800 |
GeneticVariation |
GWASCAT |
Variants in ELL2 influencing immunoglobulin levels associate with multiple myeloma.
|
26007630 |
2015 |
rs2272007
|
|
A |
0.800 |
GeneticVariation |
GWASCAT |
The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma.
|
23502783 |
2013 |
rs2272007
|
|
|
0.800 |
GeneticVariation |
GWASDB |
The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma.
|
23502783 |
2013 |
rs2272007
|
|
A |
0.800 |
GeneticVariation |
GWASDB |
Common variation at 3q26.2, 6p21.33, 17p11.2 and 22q13.1 influences multiple myeloma risk.
|
23955597 |
2013 |
rs6599175
|
|
G |
0.800 |
GeneticVariation |
GWASDB |
Common variation at 3q26.2, 6p21.33, 17p11.2 and 22q13.1 influences multiple myeloma risk.
|
23955597 |
2013 |
rs6599175
|
|
G |
0.800 |
GeneticVariation |
GWASCAT |
The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma.
|
23502783 |
2013 |
rs6599175
|
|
|
0.800 |
GeneticVariation |
GWASDB |
The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma.
|
23502783 |
2013 |
rs2272007
|
|
|
0.800 |
GeneticVariation |
GWASDB |
Common variation at 3p22.1 and 7p15.3 influences multiple myeloma risk.
|
22120009 |
2011 |
rs6599175
|
|
|
0.800 |
GeneticVariation |
GWASDB |
Common variation at 3p22.1 and 7p15.3 influences multiple myeloma risk.
|
22120009 |
2011 |
rs6599192
|
|
|
0.800 |
GeneticVariation |
GWASDB |
Common variation at 3p22.1 and 7p15.3 influences multiple myeloma risk.
|
22120009 |
2011 |
rs6763508
|
|
|
0.800 |
GeneticVariation |
GWASDB |
Common variation at 3p22.1 and 7p15.3 influences multiple myeloma risk.
|
22120009 |
2011 |
rs73071352
|
|
|
0.800 |
GeneticVariation |
GWASDB |
Common variation at 3p22.1 and 7p15.3 influences multiple myeloma risk.
|
22120009 |
2011 |
rs1125203
|
|
G |
0.700 |
GeneticVariation |
GWASDB |
Common variation at 3q26.2, 6p21.33, 17p11.2 and 22q13.1 influences multiple myeloma risk.
|
23955597 |
2013 |
rs1716975
|
|
A |
0.700 |
GeneticVariation |
GWASDB |
Common variation at 3q26.2, 6p21.33, 17p11.2 and 22q13.1 influences multiple myeloma risk.
|
23955597 |
2013 |
rs17215589
|
|
A |
0.700 |
GeneticVariation |
GWASDB |
Common variation at 3q26.2, 6p21.33, 17p11.2 and 22q13.1 influences multiple myeloma risk.
|
23955597 |
2013 |
rs1994157
|
|
A |
0.700 |
GeneticVariation |
GWASDB |
Common variation at 3q26.2, 6p21.33, 17p11.2 and 22q13.1 influences multiple myeloma risk.
|
23955597 |
2013 |
rs2128835
|
|
G |
0.700 |
GeneticVariation |
GWASDB |
Common variation at 3q26.2, 6p21.33, 17p11.2 and 22q13.1 influences multiple myeloma risk.
|
23955597 |
2013 |
rs3774372
|
|
G |
0.700 |
GeneticVariation |
GWASDB |
Common variation at 3q26.2, 6p21.33, 17p11.2 and 22q13.1 influences multiple myeloma risk.
|
23955597 |
2013 |
rs1016669
|
|
|
0.700 |
GeneticVariation |
GWASDB |
Common variation at 3p22.1 and 7p15.3 influences multiple myeloma risk.
|
22120009 |
2011 |