DisGeNET - a database of gene-disease associations

ROR1, receptor tyrosine kinase like orphan receptor 1, 4919

N. diseases: 109; N. variants: 19

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:

rs12135035

Entrez Id:	4919
Gene Symbol:	ROR1

ROR1

CUI:	C2985280
Disease:

Blood Protein Measurement

0.700

GeneticVariation

GWASCAT

Co-regulatory networks of human serum proteins link genetics to disease.

30072576

2018

dbSNP:

rs1408416

Entrez Id:	4919;101927034
Gene Symbol:	ROR1;ROR1-AS1

ROR1;ROR1-AS1

CUI:	C2985280
Disease:

Blood Protein Measurement

0.700

GeneticVariation

GWASCAT

Genomic atlas of the human plasma proteome.

29875488

2018

dbSNP:

rs6671162

Entrez Id:	4919;101927034
Gene Symbol:	ROR1;ROR1-AS1

ROR1;ROR1-AS1

CUI:	C2985280
Disease:

Blood Protein Measurement

0.700

GeneticVariation

GWASCAT

Co-regulatory networks of human serum proteins link genetics to disease.

30072576

2018

dbSNP:

rs10889450

Entrez Id:	4919
Gene Symbol:	ROR1

ROR1

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:

rs11208300

Entrez Id:	4919
Gene Symbol:	ROR1

ROR1

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:

rs11208305

Entrez Id:	4919
Gene Symbol:	ROR1

ROR1

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:

rs11581982

Entrez Id:	4919
Gene Symbol:	ROR1

ROR1

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:

rs11581982

Entrez Id:	4919
Gene Symbol:	ROR1

ROR1

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:

rs1324359

Entrez Id:	4919;101927034
Gene Symbol:	ROR1;ROR1-AS1

ROR1;ROR1-AS1

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:

rs1390116

Entrez Id:	4919
Gene Symbol:	ROR1

ROR1

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:

rs582428

Entrez Id:	4919
Gene Symbol:	ROR1

ROR1

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:

rs619334

Entrez Id:	4919
Gene Symbol:	ROR1

ROR1

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:

rs631029

Entrez Id:	4919
Gene Symbol:	ROR1

ROR1

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:

rs636119

Entrez Id:	4919
Gene Symbol:	ROR1

ROR1

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:

rs649195

Entrez Id:	4919
Gene Symbol:	ROR1

ROR1

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:

rs6588083

Entrez Id:	4919;101927034
Gene Symbol:	ROR1;ROR1-AS1

ROR1;ROR1-AS1

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:

rs675893

Entrez Id:	4919
Gene Symbol:	ROR1

ROR1

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:

rs679386

Entrez Id:	4919
Gene Symbol:	ROR1

ROR1

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:

rs1553163562

Entrez Id:	4919
Gene Symbol:	ROR1

ROR1

CUI:	C4539997
Disease:

DEAFNESS, AUTOSOMAL RECESSIVE 108

0.700

GeneticVariation

UNIPROT

ROR1 is essential for proper innervation of auditory hair cells and hearing in humans and mice.

27162350

2016

dbSNP:

rs760789417

Entrez Id:	4919
Gene Symbol:	ROR1

ROR1

CUI:	C0006142
Disease:

Malignant neoplasm of breast

0.700

GeneticVariation

UNIPROT