rs1979277, SHMT1

N. diseases: 45
Disease: Laryngeal Diseases ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Laryngeal Diseases
CUI: C0023051
Disease: Laryngeal Diseases
0.010 GeneticVariation BEFREE SHMT1 C1420T and DNMT3B C46359T polymorphisms are not associated with HNC development in Brazilian population, however, SHMT1 C1420T polymorphism is less frequent in patients with primary site of tumor in larynx and more frequent in individuals who consume tobacco and alcohol together. 24362509 2014