rs16901979, PCAT1;CASC19

N. diseases: 16
Disease: Hodgkin Disease ×
Source: BEFREE ×
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Hodgkin Disease
CUI: C0019829
Disease: Hodgkin Disease
0.010 GeneticVariation BEFREE The probands who were carriers of SNP rs16901979 (8q24) were significantly more likely to report a family history of melanoma (P = .03), and the probands with a family history of multiple myeloma and non-Hodgkin's disease were significantly more likely to be carriers of SNP rs12621278 (2q31, P = .04) and rs6465657 (7q21, P = .02), respectively. 21820706 2011