Source: CLINVAR

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121913482
rs121913482
FGFR3
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: rs121913482
rs121913482
FGFR3
CUI: C0026764
Disease: Multiple Myeloma
Multiple Myeloma 		T 0.700 CausalMutation CLINVAR