rs17601696, None

N. diseases: 2
Disease: Swallowing problem ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Swallowing problem
CUI: C0392678
Disease: Swallowing problem
0.010 GeneticVariation BEFREE SNP rs17601696 may have an impact on swallowing impairment among elderly individuals. 26116289 2015