Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 22
rs4402960 0.724 0.400 3 185793899 intron variant G/T snv 0.38 21
rs4607517
GCK
0.882 0.080 7 44196069 intron variant G/A;C snv 8
rs9356744 0.882 0.120 6 20685255 intron variant T/C snv 0.42 7