rs872071
×
Entrez Id:
3662
Gene Symbol:
IRF4
IRF4
Chronic Lymphocytic Leukemia
G
0.840
GeneticVariation
GWASCAT
A genome-wide association study identifies multiple susceptibility loci for chronic lymphocytic leukemia.
24292274
2014
rs872071
×
Entrez Id:
3662
Gene Symbol:
IRF4
IRF4
Chronic Lymphocytic Leukemia
G
0.840
GeneticVariation
GWASDB
A genome-wide association study identifies multiple susceptibility loci for chronic lymphocytic leukemia.
24292274
2014
rs872071
×
Entrez Id:
3662
Gene Symbol:
IRF4
IRF4
Chronic Lymphocytic Leukemia
G
0.840
GeneticVariation
GWASCAT
Genome-wide association study identifies multiple risk loci for chronic lymphocytic leukemia.
23770605
2013
rs872071
×
Entrez Id:
3662
Gene Symbol:
IRF4
IRF4
Chronic Lymphocytic Leukemia
G
0.840
GeneticVariation
GWASDB
Genome-wide association study identifies multiple risk loci for chronic lymphocytic leukemia.
23770605
2013
rs872071
×
Entrez Id:
3662
Gene Symbol:
IRF4
IRF4
Chronic Lymphocytic Leukemia
G
0.840
GeneticVariation
GWASDB
Common variation at 6p21.31 (BAK1) influences the risk of chronic lymphocytic leukemia.
22700719
2012
rs872071
×
Entrez Id:
3662
Gene Symbol:
IRF4
IRF4
Chronic Lymphocytic Leukemia
G
0.840
GeneticVariation
GWASCAT
Common variation at 6p21.31 (BAK1) influences the risk of chronic lymphocytic leukemia.
22700719
2012
rs872071
×
Entrez Id:
3662
Gene Symbol:
IRF4
IRF4
Chronic Lymphocytic Leukemia
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
×
Entrez Id:
3662
Gene Symbol:
IRF4
IRF4
Chronic Lymphocytic Leukemia
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
×
Entrez Id:
3662
Gene Symbol:
IRF4
IRF4
Chronic Lymphocytic Leukemia
0.840
GeneticVariation
BEFREE
We have recently shown that the IRF4 variant rs872071 influences CLL risk.
19804451
2010
rs872071
×
Entrez Id:
3662
Gene Symbol:
IRF4
IRF4
Chronic Lymphocytic Leukemia
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
×
Entrez Id:
3662
Gene Symbol:
IRF4
IRF4
Chronic Lymphocytic Leukemia
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
×
Entrez Id:
3662
Gene Symbol:
IRF4
IRF4
Chronic Lymphocytic Leukemia
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
rs12203592
×
Entrez Id:
3662
Gene Symbol:
IRF4
IRF4
Eye Color
0.800
GeneticVariation
GWASCAT
Multitrait genome association analysis identifies new susceptibility genes for human anthropometric variation in the GCAT cohort.
30166351
2018
rs12203592
×
Entrez Id:
3662
Gene Symbol:
IRF4
IRF4
Hair Color
C
0.800
GeneticVariation
GWASCAT
Genome-wide association studies identify several new loci associated with pigmentation traits and skin cancer risk in European Americans.
23548203
2013
rs12203592
×
Entrez Id:
3662
Gene Symbol:
IRF4
IRF4
Hair Color
C
0.800
GeneticVariation
GWASDB
Genome-wide association studies identify several new loci associated with pigmentation traits and skin cancer risk in European Americans.
23548203
2013
rs1050976
×
Entrez Id:
3662
Gene Symbol:
IRF4
IRF4
Celiac Disease
0.800
GeneticVariation
GWASCAT
Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease.
22057235
2011
rs1050976
×
Entrez Id:
3662
Gene Symbol:
IRF4
IRF4
Celiac Disease
0.800
GeneticVariation
GWASDB
Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease.
22057235
2011
rs12203592
×
Entrez Id:
3662
Gene Symbol:
IRF4
IRF4
Progressive supranuclear palsy
0.800
GeneticVariation
GWASDB
Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy.
21685912
2011
rs12203592
×
Entrez Id:
3662
Gene Symbol:
IRF4
IRF4
Progressive supranuclear palsy
0.800
GeneticVariation
GWASCAT
Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy.
21685912
2011
rs12203592
×
Entrez Id:
3662
Gene Symbol:
IRF4
IRF4
Eye Color
T
0.800
GeneticVariation
GWASDB
Web-based, participant-driven studies yield novel genetic associations for common traits.
20585627
2010
rs12203592
×
Entrez Id:
3662
Gene Symbol:
IRF4
IRF4
Hair Color
T
0.800
GeneticVariation
GWASCAT
Web-based, participant-driven studies yield novel genetic associations for common traits.
20585627
2010
rs12203592
×
Entrez Id:
3662
Gene Symbol:
IRF4
IRF4
Eye Color
T
0.800
GeneticVariation
GWASCAT
Web-based, participant-driven studies yield novel genetic associations for common traits.
20585627
2010
rs12203592
×
Entrez Id:
3662
Gene Symbol:
IRF4
IRF4
Hair Color
T
0.800
GeneticVariation
GWASDB
Web-based, participant-driven studies yield novel genetic associations for common traits.
20585627
2010
rs12203592
×
Entrez Id:
3662
Gene Symbol:
IRF4
IRF4
Hair Color
T
0.800
GeneticVariation
GWASDB
After adjustment for rs12203592 , the association between rs1540771 and hair color was not significant (p = 0.52).
18483556
2008
rs12203592
×
Entrez Id:
3662
Gene Symbol:
IRF4
IRF4
Hair Color
T
0.800
GeneticVariation
GWASCAT
After adjustment for rs12203592 , the association between rs1540771 and hair color was not significant (p = 0.52).
18483556
2008