Source: INFERRED ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs17851045
rs17851045
A 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016

dbSNP: rs770248150
rs770248150
G 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016

dbSNP: rs121913240
rs121913240
A 0.700 GeneticVariation CLINVAR

dbSNP: rs121913527
rs121913527
G 0.700 GeneticVariation CLINVAR

dbSNP: rs121913529
rs121913529
G 0.700 CausalMutation CLINVAR