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
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
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
rs2925979
CMIP
1.000 0.080 16 81501185 intron variant T/A;C snv 10
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv 19
rs58542926
TM6SF2
0.630 0.440 19 19268740 missense variant C/T snv 6.5E-02 5.8E-02 5
rs3794991
GATAD2A
1.000 0.080 19 19499787 intron variant C/G;T snv 7.4E-02 5
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
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 23
rs2304130
ZNF101
1.000 0.080 19 19678719 splice region variant A/G snv 0.10 0.12 5
rs7607980
COBLL1
1.000 0.080 2 164694691 missense variant T/C snv 0.11 0.13 7
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 36
rs9686661
C5orf67
1.000 0.080 5 56565959 intron variant C/T snv 0.20 3
rs9687833
C5orf67
1.000 0.080 5 56565774 intron variant G/A snv 0.21 3
rs17411031 0.925 0.120 8 19994799 regulatory region variant C/G snv 0.25 6
rs2070895
LIPC ; ALDH1A2
0.807 0.120 15 58431740 intron variant G/A snv 0.33 12
rs8108269 1.000 0.080 19 45655255 downstream gene variant T/G snv 0.35 2
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 25
rs13389219
COBLL1
1.000 0.080 2 164672366 intron variant C/T snv 0.47 8
rs10195252
COBLL1
0.925 0.080 2 164656581 intron variant T/C snv 0.48 6
rs10184004 1.000 0.080 2 164651879 downstream gene variant C/T snv 0.48 5
rs9989419 0.882 0.120 16 56951227 regulatory region variant A/G snv 0.55 10
rs11048456
LOC105369705
1.000 0.080 12 26310149 intron variant C/T snv 0.62 6