DisGeNET - a database of gene-disease associations

LINC01358, long intergenic non-protein coding RNA 1358, 101926925

N. diseases: 6; N. variants: 30

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:

rs11207423

Entrez Id:	101926925
Gene Symbol:	LINC01358

LINC01358

CUI:	C0871470
Disease:

Systolic Pressure

0.700

GeneticVariation

GWASCAT

Leveraging Polygenic Functional Enrichment to Improve GWAS Power.

30595370

2019

dbSNP:

rs34370185

Entrez Id:	101926925
Gene Symbol:	LINC01358

LINC01358

CUI:	C0428883
Disease:

Diastolic blood pressure

0.700

GeneticVariation

GWASCAT

Trans-ethnic association study of blood pressure determinants in over 750,000 individuals.

30578418

2019

dbSNP:

rs6668586

Entrez Id:	101926925
Gene Symbol:	LINC01358

LINC01358

CUI:	C0021704
Disease:

Intelligence

0.700

GeneticVariation

GWASCAT

A combined analysis of genetically correlated traits identifies 187 loci and a role for neurogenesis and myelination in intelligence.

29326435

2019

dbSNP:

rs1831539

Entrez Id:	101926925
Gene Symbol:	LINC01358

LINC01358

CUI:	C0021704
Disease:

Intelligence

0.700

GeneticVariation

GWASCAT

Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence.

29942086

2018

dbSNP:

rs1831539

Entrez Id:	101926925
Gene Symbol:	LINC01358

LINC01358

CUI:	C0021704
Disease:

Intelligence

0.700

GeneticVariation

GWASCAT

Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function.

29844566

2018

dbSNP:

rs1831539

Entrez Id:	101926925
Gene Symbol:	LINC01358

LINC01358

CUI:	C0596887
Disease:

mathematical ability

0.700

GeneticVariation

GWASCAT

Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals.

30038396

2018

dbSNP:

rs2989868

Entrez Id:	101926925
Gene Symbol:	LINC01358

LINC01358

CUI:	C0596887
Disease:

mathematical ability

0.700

GeneticVariation

GWASCAT

Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals.

30038396

2018

dbSNP:

rs2989871

Entrez Id:	101926925
Gene Symbol:	LINC01358

LINC01358

CUI:	C0596887
Disease:

mathematical ability

0.700

GeneticVariation

GWASCAT

Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals.

30038396

2018

dbSNP:

rs10493260

Entrez Id:	101926925
Gene Symbol:	LINC01358

LINC01358

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:

rs10789075

Entrez Id:	101926925
Gene Symbol:	LINC01358

LINC01358

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:

rs11207408

Entrez Id:	101926925
Gene Symbol:	LINC01358

LINC01358

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:

rs12145786

Entrez Id:	729467;101926925
Gene Symbol:	HSD52;LINC01358

HSD52;LINC01358

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:

rs1324664

Entrez Id:	101926925
Gene Symbol:	LINC01358

LINC01358

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:

rs17118797

Entrez Id:	101926925
Gene Symbol:	LINC01358

LINC01358

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:

rs17118854

Entrez Id:	729467;101926925
Gene Symbol:	HSD52;LINC01358

HSD52;LINC01358

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:

rs2985499

Entrez Id:	101926925
Gene Symbol:	LINC01358

LINC01358

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:

rs2989864

Entrez Id:	101926925
Gene Symbol:	LINC01358

LINC01358

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:

rs2989870

Entrez Id:	729467;101926925
Gene Symbol:	HSD52;LINC01358

HSD52;LINC01358

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:

rs3010332

Entrez Id:	729467;101926925
Gene Symbol:	HSD52;LINC01358

HSD52;LINC01358

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:

rs3124643

Entrez Id:	729467;101926925
Gene Symbol:	HSD52;LINC01358

HSD52;LINC01358

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:

rs332227

Entrez Id:	101926925
Gene Symbol:	LINC01358

LINC01358

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:

rs332230

Entrez Id:	101926925
Gene Symbol:	LINC01358

LINC01358

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:

rs332230

Entrez Id:	101926925
Gene Symbol:	LINC01358

LINC01358

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:

rs3898691

Entrez Id:	101926925
Gene Symbol:	LINC01358

LINC01358

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:

rs3902349

Entrez Id:	729467;101926925
Gene Symbol:	HSD52;LINC01358

HSD52;LINC01358

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