Source: CLINVAR

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs397516979
rs397516979
ERBB2 ; MIR4728
CUI: C1458155
Disease: Mammary Neoplasms
Mammary Neoplasms 		GTGT 0.700 GeneticVariation CLINVAR Prospective enterprise-level molecular genotyping of a cohort of cancer patients. 25157968

2014