DisGeNET - a database of gene-disease associations

Cerebral Infarction, C0007785

Variant: rs2106261 ×

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

Variant

Gene

Risk Allele

Score _vda

Association Type

Original DB

Sentence supporting the association

PMID

PMID Year

dbSNP:

rs2106261

rs2106261

ZFHX3

0.010

GeneticVariation

BEFREE

LT was also associated with rs</span>2106261</span> (AA+AG/GG, OR=1</span>.99, 95%CI: 1.31-3.01, p=0.001).

2017