Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121909229
rs121909229
CUI: C1458155
Disease: Mammary Neoplasms
Mammary Neoplasms
C 0.710 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016

dbSNP: rs121909229
rs121909229
CUI: C1458155
Disease: Mammary Neoplasms
Mammary Neoplasms
T 0.710 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016

dbSNP: rs121909229
rs121909229
CUI: C1458155
Disease: Mammary Neoplasms
Mammary Neoplasms
A 0.710 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011

2016