Disease: Multiple Myeloma ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs16901979
rs16901979
Entrez Id: 100750225;103021165
Gene Symbol: PCAT1;CASC19
PCAT1;CASC19
CUI: C0026764
Disease:
Multiple Myeloma 		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