TRIM46, tripartite motif containing 46, 80128

N. diseases: 17; N. variants: 7
Disease: Malignant neoplasm of stomach ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs9426886
rs9426886
Entrez Id: 80128
Gene Symbol: TRIM46
TRIM46
CUI: C0024623
Disease:
Malignant neoplasm of stomach 		0.010 GeneticVariation BEFREE SNP rs9426886 was associated with a decreased risk of non-cardia gastric cancer, but lost significance after adjustment for multiple testing. 24460302 2013