rs6774494

Parent Gene: MECOM

Importance: 3
Less common allele: A = 48%
More common allele: G = 52%
My Genotype: Log In
Risk Allele:

Disease/Trait: Nasopharyngeal Neoplasm

rs6774494 is associated with Nasopharyngeal Neoplasm (R) . It is reported to increased association with Nasopharyngeal carcinoma. No specific risk allele was identified in the study.