rs12732894
|
ARHGEF10L
|
Liver and Intrahepatic Biliary Tract Carcinoma
|
|
0.010 |
GeneticVariation |
BEFREE |
The genotyping analyses demonstrated a strong association of rs2244444 and rs12732894 with liver cancer.
|
30444969 |
2019 |
rs12732894
|
ARHGEF10L
|
Adult Liver Carcinoma
|
|
0.010 |
GeneticVariation |
BEFREE |
The genotyping analyses demonstrated a strong association of rs2244444 and rs12732894 with liver cancer.
|
30444969 |
2019 |
rs12732894
|
ARHGEF10L
|
Malignant neoplasm of liver
|
|
0.010 |
GeneticVariation |
BEFREE |
The genotyping analyses demonstrated a strong association of rs2244444 and rs12732894 with liver cancer.
|
30444969 |
2019 |
rs2244444
|
ARHGEF10L
|
Malignant neoplasm of liver
|
|
0.010 |
GeneticVariation |
BEFREE |
The genotyping analyses demonstrated a strong association of rs2244444 and rs12732894 with liver cancer.
|
30444969 |
2019 |
rs2244444
|
ARHGEF10L
|
Liver and Intrahepatic Biliary Tract Carcinoma
|
|
0.010 |
GeneticVariation |
BEFREE |
The genotyping analyses demonstrated a strong association of rs2244444 and rs12732894 with liver cancer.
|
30444969 |
2019 |
rs2244444
|
ARHGEF10L
|
Adult Liver Carcinoma
|
|
0.010 |
GeneticVariation |
BEFREE |
The genotyping analyses demonstrated a strong association of rs2244444 and rs12732894 with liver cancer.
|
30444969 |
2019 |
rs10788679
|
ARHGEF10L
|
Epithelial ovarian cancer
|
|
0.010 |
GeneticVariation |
BEFREE |
Other variants of interest included another in ARHGEF10L, rs10788679, which was associated with invasive serous EOC risk (OR = 1.07, p = 0.00026) and two variants in AKAP6 (A-kinase anchoring protein 6) which were associated with risk of invasive EOC (rs1955513, OR = 0.90, p = 0.00033; rs927062, OR = 0.94, p = 0.00059).
|
29979793 |
2018 |
rs10788679
|
ARHGEF10L
|
Carcinoma, Ovarian Epithelial
|
|
0.010 |
GeneticVariation |
BEFREE |
Other variants of interest included another in ARHGEF10L, rs10788679, which was associated with invasive serous EOC risk (OR = 1.07, p = 0.00026) and two variants in AKAP6 (A-kinase anchoring protein 6) which were associated with risk of invasive EOC (rs1955513, OR = 0.90, p = 0.00033; rs927062, OR = 0.94, p = 0.00059).
|
29979793 |
2018 |
rs2256787
|
ARHGEF10L
|
Epithelial ovarian cancer
|
|
0.010 |
GeneticVariation |
BEFREE |
One variant, ARHGEF10L (Rho guanine nucleotide exchange factor 10 like) rs2256787, was associated with increased endometrioid EOC risk (OR = 1.33, p = 4.46 x 10-6).
|
29979793 |
2018 |
rs2256787
|
ARHGEF10L
|
Carcinoma, Ovarian Epithelial
|
|
0.010 |
GeneticVariation |
BEFREE |
One variant, ARHGEF10L (Rho guanine nucleotide exchange factor 10 like) rs2256787, was associated with increased endometrioid EOC risk (OR = 1.33, p = 4.46 x 10-6).
|
29979793 |
2018 |
rs1109875
|
ARHGEF10L
|
Leukemia, Myelocytic, Acute
|
T |
0.700 |
GeneticVariation |
GWASCAT |
Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia.
|
27903959 |
2017 |
rs11580813
|
ARHGEF10L
|
Leukemia, Myelocytic, Acute
|
G |
0.700 |
GeneticVariation |
GWASCAT |
Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia.
|
27903959 |
2017 |
rs11800478
|
ARHGEF10L
|
Leukemia, Myelocytic, Acute
|
C |
0.700 |
GeneticVariation |
GWASCAT |
Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia.
|
27903959 |
2017 |
rs12067869
|
ARHGEF10L
|
Leukemia, Myelocytic, Acute
|
T |
0.700 |
GeneticVariation |
GWASCAT |
Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia.
|
27903959 |
2017 |
rs12143113
|
ARHGEF10L
|
Leukemia, Myelocytic, Acute
|
T |
0.700 |
GeneticVariation |
GWASCAT |
Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia.
|
27903959 |
2017 |
rs12143113
|
ARHGEF10L
|
Leukemia, Myelocytic, Acute
|
C |
0.700 |
GeneticVariation |
GWASCAT |
Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia.
|
27903959 |
2017 |
rs12565468
|
ARHGEF10L
|
Leukemia, Myelocytic, Acute
|
C |
0.700 |
GeneticVariation |
GWASCAT |
Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia.
|
27903959 |
2017 |
rs146330533
|
ARHGEF10L
|
Bipolar Disorder
|
|
0.700 |
GeneticVariation |
GWASCAT |
Genome-wide association studies of smooth pursuit and antisaccade eye movements in psychotic disorders: findings from the B-SNIP study.
|
29064472 |
2017 |
rs146330533
|
ARHGEF10L
|
Schizophrenia
|
|
0.700 |
GeneticVariation |
GWASCAT |
Genome-wide association studies of smooth pursuit and antisaccade eye movements in psychotic disorders: findings from the B-SNIP study.
|
29064472 |
2017 |
rs146330533
|
ARHGEF10L
|
Schizoaffective Disorder
|
|
0.700 |
GeneticVariation |
GWASCAT |
Genome-wide association studies of smooth pursuit and antisaccade eye movements in psychotic disorders: findings from the B-SNIP study.
|
29064472 |
2017 |
rs17469160
|
ARHGEF10L
|
Leukemia, Myelocytic, Acute
|
G |
0.700 |
GeneticVariation |
GWASCAT |
Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia.
|
27903959 |
2017 |
rs2134482
|
ARHGEF10L
|
Leukemia, Myelocytic, Acute
|
G |
0.700 |
GeneticVariation |
GWASCAT |
Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia.
|
27903959 |
2017 |
rs3766309
|
ARHGEF10L
|
Leukemia, Myelocytic, Acute
|
T |
0.700 |
GeneticVariation |
GWASCAT |
Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia.
|
27903959 |
2017 |
rs6657353
|
ARHGEF10L
|
Leukemia, Myelocytic, Acute
|
A |
0.700 |
GeneticVariation |
GWASCAT |
Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia.
|
27903959 |
2017 |
rs6665721
|
ARHGEF10L
|
Leukemia, Myelocytic, Acute
|
C |
0.700 |
GeneticVariation |
GWASCAT |
Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia.
|
27903959 |
2017 |