Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799884
GCK
1.000 0.080 7 44189469 intron variant C/T snv 0.17 4
rs4607517
GCK
0.882 0.080 7 44196069 intron variant G/A;C snv 3
rs2908289 1.000 0.080 7 44184343 intron variant G/A snv 0.20 3