Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1023835002
rs1023835002
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
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