DisGeNET - a database of gene-disease associations

ARHGEF10L, Rho guanine nucleotide exchange factor 10 like, 55160

N. diseases: 9; N. variants: 21

Source: ALL

Results per page

Gene

Disease

Variant

Source

Association Type

Semantic type

Protein Class

Disease Class

Type

Original DB

Consequence

DSI _v

DPI _v

pLI

EI _vda

EL _gda

Score _vda

PMID

PMID Year

AF_EXOME

Num. PMIDs

Num. SNPs_gda

AF_GENOME

Variant

Gene

Disease

Risk Allele

Score _vda

Association Type

Original DB

Sentence supporting the association

PMID

PMID Year

dbSNP:

rs1109875

Entrez Id:	55160
Gene Symbol:	ARHGEF10L

ARHGEF10L

CUI:	C0023467
Disease:

Leukemia, Myelocytic, Acute

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

Entrez Id:	55160
Gene Symbol:	ARHGEF10L

ARHGEF10L

CUI:	C0023467
Disease:

Leukemia, Myelocytic, Acute

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

Entrez Id:	55160
Gene Symbol:	ARHGEF10L

ARHGEF10L

CUI:	C0023467
Disease:

Leukemia, Myelocytic, Acute

0.700

GeneticVariation

GWASCAT

Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia.

27903959

2017

dbSNP:

rs12067869

Entrez Id:	55160
Gene Symbol:	ARHGEF10L

ARHGEF10L

CUI:	C0023467
Disease:

Leukemia, Myelocytic, Acute

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

Entrez Id:	55160
Gene Symbol:	ARHGEF10L

ARHGEF10L

CUI:	C0023467
Disease:

Leukemia, Myelocytic, Acute

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

Entrez Id:	55160
Gene Symbol:	ARHGEF10L

ARHGEF10L

CUI:	C0023467
Disease:

Leukemia, Myelocytic, Acute

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

Entrez Id:	55160
Gene Symbol:	ARHGEF10L

ARHGEF10L

CUI:	C0023467
Disease:

Leukemia, Myelocytic, Acute

0.700

GeneticVariation

GWASCAT

Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia.

27903959

2017

dbSNP:

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

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

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:

rs17469160

Entrez Id:	55160
Gene Symbol:	ARHGEF10L

ARHGEF10L

CUI:	C0023467
Disease:

Leukemia, Myelocytic, Acute

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

Entrez Id:	55160
Gene Symbol:	ARHGEF10L

ARHGEF10L

CUI:	C0023467
Disease:

Leukemia, Myelocytic, Acute

0.700

GeneticVariation

GWASCAT

Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia.

27903959

2017

dbSNP:

rs3766309

Entrez Id:	55160
Gene Symbol:	ARHGEF10L

ARHGEF10L

CUI:	C0023467
Disease:

Leukemia, Myelocytic, Acute

0.700

GeneticVariation

GWASCAT

Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia.

27903959

2017

dbSNP:

rs6657353

Entrez Id:	55160
Gene Symbol:	ARHGEF10L

ARHGEF10L

CUI:	C0023467
Disease:

Leukemia, Myelocytic, Acute

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

Entrez Id:	55160
Gene Symbol:	ARHGEF10L

ARHGEF10L

CUI:	C0023467
Disease:

Leukemia, Myelocytic, Acute

0.700

GeneticVariation

GWASCAT

Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia.

27903959

2017

dbSNP:

rs6703771

Entrez Id:	55160
Gene Symbol:	ARHGEF10L

ARHGEF10L

CUI:	C0023467
Disease:

Leukemia, Myelocytic, Acute

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

Entrez Id:	55160
Gene Symbol:	ARHGEF10L

ARHGEF10L

CUI:	C0023467
Disease:

Leukemia, Myelocytic, Acute

0.700

GeneticVariation

GWASCAT

Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia.

27903959

2017

dbSNP:

rs7531556

Entrez Id:	55160
Gene Symbol:	ARHGEF10L

ARHGEF10L

CUI:	C0023467
Disease:

Leukemia, Myelocytic, Acute

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

Entrez Id:	55160
Gene Symbol:	ARHGEF10L

ARHGEF10L

CUI:	C0023467
Disease:

Leukemia, Myelocytic, Acute

0.700

GeneticVariation

GWASCAT

Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia.

27903959

2017

dbSNP:

rs1421731181

Entrez Id:	55160
Gene Symbol:	ARHGEF10L

ARHGEF10L

CUI:	C0009402
Disease:

Colorectal Carcinoma

0.700

GeneticVariation

UNIPROT

dbSNP:

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

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

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

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

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