Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1421731181
rs1421731181
Entrez Id: 55160
Gene Symbol: ARHGEF10L
ARHGEF10L
CUI: C0009402
Disease:
Colorectal Carcinoma 		0.700 GeneticVariation UNIPROT
dbSNP: rs146330533
rs146330533
Entrez Id: 55160
Gene Symbol: ARHGEF10L
ARHGEF10L
CUI: C0005586
Disease:
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
dbSNP: rs146330533
rs146330533
Entrez Id: 55160
Gene Symbol: ARHGEF10L
ARHGEF10L
CUI: C0036341
Disease:
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
dbSNP: rs146330533
rs146330533
Entrez Id: 55160
Gene Symbol: ARHGEF10L
ARHGEF10L
CUI: C0036337
Disease:
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
dbSNP: rs10788679
rs10788679
Entrez Id: 55160
Gene Symbol: ARHGEF10L
ARHGEF10L
CUI: C0677886
Disease:
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
dbSNP: rs10788679
rs10788679
Entrez Id: 55160
Gene Symbol: ARHGEF10L
ARHGEF10L
CUI: C4721610
Disease:
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
dbSNP: rs12732894
rs12732894
Entrez Id: 55160
Gene Symbol: ARHGEF10L
ARHGEF10L
CUI: C0279000
Disease:
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
dbSNP: rs12732894
rs12732894
Entrez Id: 55160
Gene Symbol: ARHGEF10L
ARHGEF10L
CUI: C0220630
Disease:
Adult Liver Carcinoma 		0.010 GeneticVariation BEFREE The genotyping analyses demonstrated a strong association of rs2244444 and rs12732894 with liver cancer. 30444969 2019
dbSNP: rs12732894
rs12732894
Entrez Id: 55160
Gene Symbol: ARHGEF10L
ARHGEF10L
CUI: C0345904
Disease:
Malignant neoplasm of liver 		0.010 GeneticVariation BEFREE The genotyping analyses demonstrated a strong association of rs2244444 and rs12732894 with liver cancer. 30444969 2019
dbSNP: rs2244444
rs2244444
Entrez Id: 55160
Gene Symbol: ARHGEF10L
ARHGEF10L
CUI: C0345904
Disease:
Malignant neoplasm of liver 		0.010 GeneticVariation BEFREE The genotyping analyses demonstrated a strong association of rs2244444 and rs12732894 with liver cancer. 30444969 2019
dbSNP: rs2244444
rs2244444
Entrez Id: 55160
Gene Symbol: ARHGEF10L
ARHGEF10L
CUI: C0279000
Disease:
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
dbSNP: rs2244444
rs2244444
Entrez Id: 55160
Gene Symbol: ARHGEF10L
ARHGEF10L
CUI: C0220630
Disease:
Adult Liver Carcinoma 		0.010 GeneticVariation BEFREE The genotyping analyses demonstrated a strong association of rs2244444 and rs12732894 with liver cancer. 30444969 2019
dbSNP: rs2256787
rs2256787
Entrez Id: 55160
Gene Symbol: ARHGEF10L
ARHGEF10L
CUI: C0677886
Disease:
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
dbSNP: rs2256787
rs2256787
Entrez Id: 55160
Gene Symbol: ARHGEF10L
ARHGEF10L
CUI: C4721610
Disease:
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
dbSNP: rs6657353
rs6657353
Entrez Id: 55160
Gene Symbol: ARHGEF10L
ARHGEF10L
CUI: C0023467
Disease:
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
dbSNP: rs7528550
rs7528550
Entrez Id: 55160
Gene Symbol: ARHGEF10L
ARHGEF10L
CUI: C0023467
Disease:
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
dbSNP: rs11800478
rs11800478
Entrez Id: 55160
Gene Symbol: ARHGEF10L
ARHGEF10L
CUI: C0023467
Disease:
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
dbSNP: rs12143113
rs12143113
Entrez Id: 55160
Gene Symbol: ARHGEF10L
ARHGEF10L
CUI: C0023467
Disease:
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
dbSNP: rs12565468
rs12565468
Entrez Id: 55160
Gene Symbol: ARHGEF10L
ARHGEF10L
CUI: C0023467
Disease:
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
dbSNP: rs6665721
rs6665721
Entrez Id: 55160
Gene Symbol: ARHGEF10L
ARHGEF10L
CUI: C0023467
Disease:
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
dbSNP: rs11580813
rs11580813
Entrez Id: 55160
Gene Symbol: ARHGEF10L
ARHGEF10L
CUI: C0023467
Disease:
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
dbSNP: rs17469160
rs17469160
Entrez Id: 55160
Gene Symbol: ARHGEF10L
ARHGEF10L
CUI: C0023467
Disease:
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
dbSNP: rs2134482
rs2134482
Entrez Id: 55160
Gene Symbol: ARHGEF10L
ARHGEF10L
CUI: C0023467
Disease:
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
dbSNP: rs869526
rs869526
Entrez Id: 55160
Gene Symbol: ARHGEF10L
ARHGEF10L
CUI: C0023467
Disease:
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
dbSNP: rs1109875
rs1109875
Entrez Id: 55160
Gene Symbol: ARHGEF10L
ARHGEF10L
CUI: C0023467
Disease:
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