DisGeNET - a database of gene-disease associations

rs4968451, BRIP1

N. diseases: 13

Disease: Transitional Meningioma ×

Source: ALL

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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

Transitional Meningioma

CUI:	C0334611
Disease:	Transitional Meningioma

0.010

GeneticVariation

BEFREE

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

2018