Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31 28
rs35859249
TBC1D1
0.807 0.200 4 37902468 missense variant C/A;T snv 4.0E-06; 9.7E-02 6