Table 5.

Genetic variants of FTO with potential disease association

dbSNP ID	Induced Mutation	Clinical Significance
rs121918214	Arg316Gln	Pathogenic
rs139577103	Arg96Pro	Uncertain Significance
rs745616565	Arg322Gln	Likely Pathogenic
rs1203776934	Gly103Asp	Uncertain Significance
rs1259762053	Tyr295Cys	-