Disease: Diabetes
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17235409
SLC11A1
0.653 0.600 2 218395009 missense variant G/A;C snv 4.9E-02; 4.1E-06 31
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs35829419
NLRP3
0.689 0.560 1 247425556 missense variant C/A snv 3.9E-02 3.3E-02 23
rs2111485 0.724 0.280 2 162254026 regulatory region variant A/G snv 0.46 17
rs780093
GCKR
0.763 0.240 2 27519736 intron variant T/C snv 0.68 30
rs864745
JAZF1
0.763 0.320 7 28140937 intron variant T/C snv 0.41 12
rs1728918 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 19