Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1059292
rs1059292
SLC3A2 ; SNORD29 ; SNORD30 ; SNORD28 ; SNORD27 ; SNORD26 ; SNORD25 ; SNHG1
0.010 GeneticVariation BEFREE Our data suggest that genetic variation of rs1059292 in CD98 gene may affect clinical outcome of NSCLC in Chinese population. 24782339

2015