DisGeNET - a database of gene-disease associations

rs157935, LINC00513;LINC-PINT

N. diseases: 4

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

Disease

Risk Allele

Score _vda

Association Type

Original DB

Sentence supporting the association

PMID

PMID Year

Basal Cell Cancer

CUI:	C0751676
Disease:	Basal Cell Cancer

0.700

GeneticVariation

GWASCAT

New basal cell carcinoma susceptibility loci.

25855136

2015

Basal Cell Neoplasm

CUI:	C0206710
Disease:	Basal Cell Neoplasm

0.700

GeneticVariation

GWASCAT

New basal cell carcinoma susceptibility loci.

25855136

2015

Basal cell carcinoma

CUI:	C0007117
Disease:	Basal cell carcinoma

0.700

GeneticVariation

GWASCAT

New basal cell carcinoma susceptibility loci.

25855136

2015

Basal Cell Neoplasm

CUI:	C0206710
Disease:	Basal Cell Neoplasm

0.700

GeneticVariation

GWASCAT

Germline sequence variants in TGM3 and RGS22 confer risk of basal cell carcinoma.

24403052

2014

Basal Cell Cancer

CUI:	C0751676
Disease:	Basal Cell Cancer

0.700

GeneticVariation

GWASCAT

Germline sequence variants in TGM3 and RGS22 confer risk of basal cell carcinoma.

24403052

2014

Basal cell carcinoma

CUI:	C0007117
Disease:	Basal cell carcinoma

0.700

GeneticVariation

GWASCAT

Germline sequence variants in TGM3 and RGS22 confer risk of basal cell carcinoma.

24403052

2014

Carcinoma, Basal Cell

CUI:	C4721806
Disease:	Carcinoma, Basal Cell

0.700

GeneticVariation

GWASDB

Germline sequence variants in TGM3 and RGS22 confer risk of basal cell carcinoma.

24403052

2014