Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1121980
rs1121980
FTO
9 0.807 0.240 16 53775335 intron variant G/A;C snv 0.800 1.000 1 2013 2013
dbSNP: rs16952619
rs16952619
FTO
1 16 53884735 intron variant A/G snv 4.7E-02 0.700 1.000 1 2012 2012