DisGeNET - a database of gene-disease associations

Malignant neoplasm of stomach, C0024623

Variant: rs10474606 ×

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

Risk Allele

Score _vda

Association Type

Original DB

Sentence supporting the association

PMID

PMID Year

dbSNP:

rs10474606

rs10474606

THBS4

0.010

GeneticVariation

BEFREE

In addition, individuals carrying the THBS4 rs10474606 variant homozygous AA had a modest reduced GC risk.

2016