Source: BEFREE ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs6903608
rs6903608
HLA-DRB9
0.020 GeneticVariation BEFREE For EBV-negative cHL the class II SNP rs6903608 remained the strongest predictor of disease risk after adjusting for the effects of common HLA alleles. 25648508

2015
dbSNP: rs6903608
rs6903608
HLA-DRB9
0.020 GeneticVariation BEFREE The association between rs6903608 and EBV-negative cHL was confined to the nodular sclerosis histological subtype. 22286212

2012