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
rs2867125 0.925 0.120 2 622827 intergenic variant T/A;C snv 0.85 6
rs7202116
FTO
0.882 0.120 16 53787703 intron variant A/G snv 0.41 6
rs76895963
CCND2-AS1 ; CCND2
1.000 0.080 12 4275678 intron variant T/G snv 1.5E-02 6
rs8089364 0.925 0.120 18 60191596 upstream gene variant T/C snv 0.21 6
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 5
rs11558471
LOC105375716 ; SLC30A8
1.000 0.080 8 117173494 3 prime UTR variant A/G snv 0.25 5
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 5
rs2237892
KCNQ1
0.790 0.320 11 2818521 intron variant C/T snv 9.2E-02 5
rs2304130
ZNF101
1.000 0.080 19 19678719 splice region variant A/G snv 0.10 0.12 5
rs2307111
POC5
0.925 0.120 5 75707853 missense variant T/A;C snv 4.5E-06; 0.47 5
rs5219
KCNJ11
0.701 0.360 11 17388025 stop gained T/A;C snv 0.64 5
rs7185735
FTO
0.925 0.120 16 53788739 intron variant A/G;T snv 5
rs7193144
FTO
0.925 0.120 16 53776774 intron variant T/C snv 0.40 5
rs7570971
RAB3GAP1
1.000 0.080 2 135080336 intron variant C/A snv 0.61 5
rs8043757
FTO
0.925 0.120 16 53779538 intron variant A/T snv 0.40 5
rs9356744
CDKAL1
0.882 0.120 6 20685255 intron variant T/C snv 0.42 5
rs9936385
FTO
0.925 0.120 16 53785257 intron variant T/C snv 0.41 5
rs11257655 1.000 0.080 10 12265895 TF binding site variant C/T snv 0.23 4
rs11671664
GIPR
0.925 0.120 19 45669020 intron variant G/A snv 0.12 4
rs1470579
IGF2BP2
0.925 0.160 3 185811292 intron variant A/C snv 0.46 4
rs2191349 1.000 0.080 7 15024684 intergenic variant G/T snv 0.54 4
rs2206734
CDKAL1
0.882 0.160 6 20694653 intron variant C/T snv 0.20 4
rs2296172
MACF1
1.000 0.080 1 39370145 missense variant A/G;T snv 0.19; 8.0E-06 4
rs340874
PROX1 ; PROX1-AS1
0.882 0.080 1 213985913 non coding transcript exon variant T/C snv 0.40 4
rs3802177
SLC30A8 ; LOC105375716
1.000 0.080 8 117172786 3 prime UTR variant G/A snv 0.24 4