Source: CLINVAR

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs113488022
rs113488022
BRAF
CUI: C0026764
Disease: Multiple Myeloma
Multiple Myeloma 		T 0.770 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs78311289
rs78311289
FGFR3
CUI: C0026764
Disease: Multiple Myeloma
Multiple Myeloma 		G 0.730 CausalMutation CLINVAR

dbSNP: rs397516896
rs397516896
BRAF
CUI: C0026764
Disease: Multiple Myeloma
Multiple Myeloma 		T 0.710 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs397516896
rs397516896
BRAF
CUI: C0026764
Disease: Multiple Myeloma
Multiple Myeloma 		G 0.710 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs1023835002
rs1023835002
B2M ; PATL2
CUI: C0026764
Disease: Multiple Myeloma
Multiple Myeloma 		G 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs1023835002
rs1023835002
B2M ; PATL2
CUI: C0026764
Disease: Multiple Myeloma
Multiple Myeloma 		T 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs104894226
rs104894226
HRAS ; LRRC56
CUI: C0026764
Disease: Multiple Myeloma
Multiple Myeloma 		A 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs104894226
rs104894226
HRAS ; LRRC56
CUI: C0026764
Disease: Multiple Myeloma
Multiple Myeloma 		G 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs104894228
rs104894228
HRAS ; LRRC56
CUI: C0026764
Disease: Multiple Myeloma
Multiple Myeloma 		G 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs104894228
rs104894228
HRAS ; LRRC56
CUI: C0026764
Disease: Multiple Myeloma
Multiple Myeloma 		A 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs104894229
rs104894229
HRAS ; LRRC56
CUI: C0026764
Disease: Multiple Myeloma
Multiple Myeloma 		T 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs104894229
rs104894229
HRAS ; LRRC56
CUI: C0026764
Disease: Multiple Myeloma
Multiple Myeloma 		A 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs104894230
rs104894230
HRAS ; LRRC56
CUI: C0026764
Disease: Multiple Myeloma
Multiple Myeloma 		G 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs104894231
rs104894231
HRAS ; LRRC56
CUI: C0026764
Disease: Multiple Myeloma
Multiple Myeloma 		T 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs104894231
rs104894231
HRAS ; LRRC56
CUI: C0026764
Disease: Multiple Myeloma
Multiple Myeloma 		G 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs104894340
rs104894340
CDK4
CUI: C0026764
Disease: Multiple Myeloma
Multiple Myeloma 		A 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs104894340
rs104894340
CDK4
CUI: C0026764
Disease: Multiple Myeloma
Multiple Myeloma 		T 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs104894419
rs104894419
LIG4
CUI: C0026764
Disease: Multiple Myeloma
Multiple Myeloma 		A 0.700 CausalMutation CLINVAR

dbSNP: rs1057517992
rs1057517992
KMT2D
CUI: C0026764
Disease: Multiple Myeloma
Multiple Myeloma 		A 0.700 GeneticVariation CLINVAR

dbSNP: rs1057519877
rs1057519877
B2M ; PATL2
CUI: C0026764
Disease: Multiple Myeloma
Multiple Myeloma 		A 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs1057519879
rs1057519879
B2M ; PATL2
CUI: C0026764
Disease: Multiple Myeloma
Multiple Myeloma 		C 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs1057519879
rs1057519879
B2M ; PATL2
CUI: C0026764
Disease: Multiple Myeloma
Multiple Myeloma 		G 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs1057519933
rs1057519933
PIK3CA
CUI: C0026764
Disease: Multiple Myeloma
Multiple Myeloma 		G 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs1057519934
rs1057519934
PIK3CA
CUI: C0026764
Disease: Multiple Myeloma
Multiple Myeloma 		C 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016
dbSNP: rs1057519935
rs1057519935
PIK3CA
CUI: C0026764
Disease: Multiple Myeloma
Multiple Myeloma 		G 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016