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
rs1470579
IGF2BP2
0.925 0.160 3 185811292 intron variant A/C snv 0.46 4
rs2943634 0.763 0.200 2 226203364 intergenic variant A/C;G snv 8
rs11075990
FTO
0.925 0.120 16 53785981 intron variant A/G snv 0.41 6
rs11558471
LOC105375716 ; SLC30A8
1.000 0.080 8 117173494 3 prime UTR variant A/G snv 0.25 5
rs11708067
ADCY5
0.882 0.080 3 123346931 intron variant A/G snv 0.19 6
rs2304130
ZNF101
1.000 0.080 19 19678719 splice region variant A/G snv 0.10 0.12 5
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 36
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 20
rs7202116
FTO
0.882 0.120 16 53787703 intron variant A/G snv 0.41 6
rs7578326
LOC646736
0.882 0.080 2 226155937 TF binding site variant A/G snv 0.36 3
rs2296172
MACF1
1.000 0.080 1 39370145 missense variant A/G;T snv 0.19; 8.0E-06 4
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv 19
rs7185735
FTO
0.925 0.120 16 53788739 intron variant A/G;T snv 5
rs6947395
AUTS2
1.000 0.080 7 69941675 intron variant A/T snv 0.20 2
rs8043757
FTO
0.925 0.120 16 53779538 intron variant A/T snv 0.40 5
rs35261542
CDKAL1
1.000 0.080 6 20675561 intron variant C/A snv 0.26 3
rs7570971
RAB3GAP1
1.000 0.080 2 135080336 intron variant C/A snv 0.61 5
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 16
rs7034200
GLIS3
1.000 0.080 9 4289050 intron variant C/A;G snv 3
rs7020996 0.925 0.120 9 22129580 downstream gene variant C/A;T snv 3
rs9368222
CDKAL1
1.000 0.080 6 20686765 intron variant C/A;T snv 8
rs10830963
MTNR1B
0.776 0.400 11 92975544 intron variant C/G snv 0.22 10
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 5
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 19
rs11257655 1.000 0.080 10 12265895 TF binding site variant C/T snv 0.23 4