rs735665
|
|
|
0.840 |
GeneticVariation |
BEFREE |
The haplotype tagged by rs35923643-G (or its proxy SNP rs735665-A) is also known as the top risk allele for chronic lymphocytic leukemia (CLL), and a main increasing allele for general IgM.
|
29547969 |
2018 |
rs735665
|
|
A |
0.840 |
GeneticVariation |
GWASCAT |
A genome-wide association study identifies multiple susceptibility loci for chronic lymphocytic leukemia.
|
24292274 |
2014 |
rs735665
|
|
A |
0.840 |
GeneticVariation |
GWASDB |
A genome-wide association study identifies multiple susceptibility loci for chronic lymphocytic leukemia.
|
24292274 |
2014 |
rs872071
|
|
G |
0.840 |
GeneticVariation |
GWASCAT |
A genome-wide association study identifies multiple susceptibility loci for chronic lymphocytic leukemia.
|
24292274 |
2014 |
rs872071
|
|
G |
0.840 |
GeneticVariation |
GWASDB |
A genome-wide association study identifies multiple susceptibility loci for chronic lymphocytic leukemia.
|
24292274 |
2014 |
rs735665
|
|
A |
0.840 |
GeneticVariation |
GWASCAT |
Genome-wide association study identifies multiple risk loci for chronic lymphocytic leukemia.
|
23770605 |
2013 |
rs735665
|
|
A |
0.840 |
GeneticVariation |
GWASDB |
Genome-wide association study identifies multiple risk loci for chronic lymphocytic leukemia.
|
23770605 |
2013 |
rs872071
|
|
G |
0.840 |
GeneticVariation |
GWASCAT |
Genome-wide association study identifies multiple risk loci for chronic lymphocytic leukemia.
|
23770605 |
2013 |
rs872071
|
|
G |
0.840 |
GeneticVariation |
GWASDB |
Genome-wide association study identifies multiple risk loci for chronic lymphocytic leukemia.
|
23770605 |
2013 |
rs735665
|
|
A |
0.840 |
GeneticVariation |
GWASDB |
Common variation at 6p21.31 (BAK1) influences the risk of chronic lymphocytic leukemia.
|
22700719 |
2012 |
rs735665
|
|
A |
0.840 |
GeneticVariation |
GWASCAT |
Common variation at 6p21.31 (BAK1) influences the risk of chronic lymphocytic leukemia.
|
22700719 |
2012 |
rs872071
|
|
G |
0.840 |
GeneticVariation |
GWASDB |
Common variation at 6p21.31 (BAK1) influences the risk of chronic lymphocytic leukemia.
|
22700719 |
2012 |
rs872071
|
|
G |
0.840 |
GeneticVariation |
GWASCAT |
Common variation at 6p21.31 (BAK1) influences the risk of chronic lymphocytic leukemia.
|
22700719 |
2012 |
rs735665
|
|
|
0.840 |
GeneticVariation |
BEFREE |
Common single nucleotide polymorphisms (SNPs) at 2q13 (rs17483466), 2q37.1 (rs13397985), 2q37.3 (rs757978), 6p25.3 (rs872071), 8q24.21 (rs2456449), 11q24.1 (rs735665), 15q21.3 (rs7169431), 15q23 (rs7176508), 16q24.1 (rs305061), and 19q13.32 (rs11083846) have been shown to confer a modest but significant increase in CLL risk.
|
20855867 |
2010 |
rs735665
|
|
|
0.840 |
GeneticVariation |
BEFREE |
Combined data provided statistically significant support for an association between genotypes at rs13397985, rs872071, rs735665, rs7176508 and rs11083846 and CLL risk.
|
20553269 |
2010 |
rs872071
|
|
|
0.840 |
GeneticVariation |
BEFREE |
A recent genome wide association study of chronic lymphocytic leukaemia (CLL) provided evidence that common variation at 2q13 (rs17483466), 2q37.1 (rs13397985), 6p25.3 (rs872071), 11q24.1 (rs735665), 15q23 (rs7176508) and 19q13.32 (rs11083846) affects CLL risk.
|
20553269 |
2010 |
rs872071
|
|
|
0.840 |
GeneticVariation |
BEFREE |
Common single nucleotide polymorphisms (SNPs) at 2q13 (rs17483466), 2q37.1 (rs13397985), 2q37.3 (rs757978), 6p25.3 (rs872071), 8q24.21 (rs2456449), 11q24.1 (rs735665), 15q21.3 (rs7169431), 15q23 (rs7176508), 16q24.1 (rs305061), and 19q13.32 (rs11083846) have been shown to confer a modest but significant increase in CLL risk.
|
20855867 |
2010 |
rs872071
|
|
|
0.840 |
GeneticVariation |
BEFREE |
We have recently shown that the IRF4 variant rs872071 influences CLL risk.
|
19804451 |
2010 |
rs735665
|
|
A |
0.840 |
GeneticVariation |
GWASCAT |
We identified six previously unreported CLL risk loci at 2q13 (rs17483466; P = 2.36 x 10(-10)), 2q37.1 (rs13397985, SP140; P = 5.40 x 10(-10)), 6p25.3 (rs872071, IRF4; P = 1.91 x 10(-20)), 11q24.1 (rs735665; P = 3.78 x 10(-12)), 15q23 (rs7176508; P = 4.54 x 10(-12)) and 19q13.32 (rs11083846, PRKD2; P = 3.96 x 10(-9)).
|
18758461 |
2008 |
rs735665
|
|
|
0.840 |
GeneticVariation |
BEFREE |
We identified six previously unreported CLL risk loci at 2q13 (rs17483466; P = 2.36 x 10(-10)), 2q37.1 (rs13397985, SP140; P = 5.40 x 10(-10)), 6p25.3 (rs872071, IRF4; P = 1.91 x 10(-20)), 11q24.1 (rs735665; P = 3.78 x 10(-12)), 15q23 (rs7176508; P = 4.54 x 10(-12)) and 19q13.32 (rs11083846, PRKD2; P = 3.96 x 10(-9)).
|
18758461 |
2008 |
rs735665
|
|
A |
0.840 |
GeneticVariation |
GWASDB |
We identified six previously unreported CLL risk loci at 2q13 (rs17483466; P = 2.36 x 10(-10)), 2q37.1 (rs13397985, SP140; P = 5.40 x 10(-10)), 6p25.3 (rs872071, IRF4; P = 1.91 x 10(-20)), 11q24.1 (rs735665; P = 3.78 x 10(-12)), 15q23 (rs7176508; P = 4.54 x 10(-12)) and 19q13.32 (rs11083846, PRKD2; P = 3.96 x 10(-9)).
|
18758461 |
2008 |
rs872071
|
|
|
0.840 |
GeneticVariation |
BEFREE |
We identified six previously unreported CLL risk loci at 2q13 (rs17483466; P = 2.36 x 10(-10)), 2q37.1 (rs13397985, SP140; P = 5.40 x 10(-10)), 6p25.3 (rs872071, IRF4; P = 1.91 x 10(-20)), 11q24.1 (rs735665; P = 3.78 x 10(-12)), 15q23 (rs7176508; P = 4.54 x 10(-12)) and 19q13.32 (rs11083846, PRKD2; P = 3.96 x 10(-9)).
|
18758461 |
2008 |
rs872071
|
|
G |
0.840 |
GeneticVariation |
GWASCAT |
We identified six previously unreported CLL risk loci at 2q13 (rs17483466; P = 2.36 x 10(-10)), 2q37.1 (rs13397985, SP140; P = 5.40 x 10(-10)), 6p25.3 (rs872071, IRF4; P = 1.91 x 10(-20)), 11q24.1 (rs735665; P = 3.78 x 10(-12)), 15q23 (rs7176508; P = 4.54 x 10(-12)) and 19q13.32 (rs11083846, PRKD2; P = 3.96 x 10(-9)).
|
18758461 |
2008 |
rs872071
|
|
G |
0.840 |
GeneticVariation |
GWASDB |
We identified six previously unreported CLL risk loci at 2q13 (rs17483466; P = 2.36 x 10(-10)), 2q37.1 (rs13397985, SP140; P = 5.40 x 10(-10)), 6p25.3 (rs872071, IRF4; P = 1.91 x 10(-20)), 11q24.1 (rs735665; P = 3.78 x 10(-12)), 15q23 (rs7176508; P = 4.54 x 10(-12)) and 19q13.32 (rs11083846, PRKD2; P = 3.96 x 10(-9)).
|
18758461 |
2008 |
rs13397985
|
|
G |
0.830 |
GeneticVariation |
GWASCAT |
A genome-wide association study identifies multiple susceptibility loci for chronic lymphocytic leukemia.
|
24292274 |
2014 |