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: rs11075992
rs11075992
FTO
3 1.000 0.080 16 53786154 intron variant T/C snv 0.41 0.700 1.000 1 2019 2019
dbSNP: rs1421085
rs1421085
FTO
28 0.752 0.280 16 53767042 intron variant T/C snv 0.31 0.700 1.000 1 2019 2019