Disease: Multiple Myeloma ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1948915
rs1948915
Entrez Id: 100507056;100750225;103021165
Gene Symbol: CCAT1;PCAT1;CASC19
CCAT1;PCAT1;CASC19
CUI: C0026764
Disease:
Multiple Myeloma 		C 0.700 GeneticVariation GWASCAT Genome-wide association study identifies multiple susceptibility loci for multiple myeloma. 27363682 2016
dbSNP: rs2456449
rs2456449
Entrez Id: 100750225;103021165
Gene Symbol: PCAT1;CASC19
PCAT1;CASC19
CUI: C0026764
Disease:
Multiple Myeloma 		0.010 GeneticVariation BEFREE We genotyped 20 single nucleotide polymorphisms of 8q24 in 1188 MM cases and 2465 controls and found a statistically significant (P = 0·0022) association between rs2456449 and MM risk. 22590720 2012
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