DisGeNET - a database of gene-disease associations

Source: ALL

Disease: Transitional Meningioma ×

Variant: rs4968451 ×

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:

rs4968451

rs4968451

BRIP1

CUI:	C0334611
Disease:	Transitional Meningioma

Transitional Meningioma

0.010

GeneticVariation

BEFREE

In addition, BRIP1 rs4968451T>G was associated with markedly meningothelial and transitional meningioma risk.

2018