DisGeNET - a database of gene-disease associations

rs1051740, EPHX1

N. diseases: 56

Disease: Childhood Medulloblastoma ×

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

Childhood Medulloblastoma

CUI:	C0278510
Disease:	Childhood Medulloblastoma

0.010

GeneticVariation

BEFREE

However, the maternal EPHX1 rs1051740 genotype (RR = 3.26, P = .01) was associated with medulloblastoma risk.

2012