Disease: Diabetes Mellitus, Non-Insulin-Dependent
Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 64
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 43
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 36
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 25
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 23
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 20
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv 19
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 18
rs2070895
LIPC ; ALDH1A2
0.807 0.120 15 58431740 intron variant G/A snv 0.33 12
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 11
rs1128249
COBLL1
1.000 0.080 2 164672114 intron variant G/C;T snv 10
rs2925979
CMIP
1.000 0.080 16 81501185 intron variant T/A;C snv 10
rs9989419 0.882 0.120 16 56951227 regulatory region variant A/G snv 0.55 10
rs459193
C5orf67
0.925 0.120 5 56510924 downstream gene variant A/G snv 0.69 9
rs13389219
COBLL1
1.000 0.080 2 164672366 intron variant C/T snv 0.47 8
rs17482753 1.000 0.080 8 19975135 regulatory region variant G/T snv 8.8E-02 8
rs328
LPL
0.732 0.440 8 19962213 stop gained C/G snv 9.2E-02 9.0E-02 8
rs12454712
BCL2
0.925 0.120 18 63178651 intron variant T/A;C snv 7
rs13266634
SLC30A8 ; LOC105375716
0.724 0.480 8 117172544 missense variant C/A;T snv 0.29 7
rs2943641 0.763 0.160 2 226229029 intergenic variant T/C snv 0.67 7
rs7607980
COBLL1
1.000 0.080 2 164694691 missense variant T/C snv 0.11 0.13 7
rs10195252
COBLL1
0.925 0.080 2 164656581 intron variant T/C snv 0.48 6
rs11048456
LOC105369705
1.000 0.080 12 26310149 intron variant C/T snv 0.62 6
rs17411031 0.925 0.120 8 19994799 regulatory region variant C/G snv 0.25 6
rs10184004 1.000 0.080 2 164651879 downstream gene variant C/T snv 0.48 5