DisGeNET - a database of gene-disease associations

PIGN, phosphatidylinositol glycan anchor biosynthesis class N, 23556

N. diseases: 173; N. variants: 25

Disease: Paget Disease ×

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:

rs4941107

Entrez Id:	23556
Gene Symbol:	PIGN

PIGN

CUI:	C1368019
Disease:

Paget Disease

0.700

GeneticVariation

GWASDB

Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone.

20436471

2010

dbSNP:

rs663354

Entrez Id:	23556
Gene Symbol:	PIGN

PIGN

CUI:	C1368019
Disease:

Paget Disease

0.700

GeneticVariation

GWASDB

Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone.

20436471

2010

dbSNP:

rs9636100

Entrez Id:	23556
Gene Symbol:	PIGN

PIGN

CUI:	C1368019
Disease:

Paget Disease

0.700

GeneticVariation

GWASDB

Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone.

20436471

2010