Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4430796
HNF1B
0.790 0.280 17 37738049 intron variant A/G snv 0.52 14
rs4586
CCL2
0.790 0.280 17 34256250 synonymous variant T/C snv 0.44 0.48 8
rs5435
SLC2A4
0.851 0.200 17 7283804 missense variant T/A;C snv 0.65 6
rs391300
SRR
0.882 0.160 17 2312964 intron variant T/C snv 0.58 4
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 32
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31 28
rs1232880706
FBN1
0.689 0.440 15 48526247 stop gained C/A;T snv 36
rs7178572
HMG20A
0.925 0.120 15 77454848 intron variant A/G snv 0.63 3
rs736118
STRA6
1.000 0.080 15 74181398 missense variant C/G;T snv 0.16 2
rs351219
STRA6
15 74196866 intron variant T/C snv 0.44 1
rs1400419650
TRIP11
0.708 0.320 14 92005938 stop gained C/A;T snv 4.0E-06 1.4E-05 38
rs1555386022
TRIP11
0.708 0.320 14 92003418 splice donor variant C/A snv 38
rs1805097
IRS2
0.689 0.360 13 109782884 missense variant C/G;T snv 0.35 22
rs192902098
PDX1
1.000 0.040 13 27920235 missense variant C/A;G;T snv 2.6E-03; 3.4E-04; 5.6E-05 3
rs5443
CDCA3 ; GNB3
0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs731236
VDR
0.542 0.760 12 47844974 synonymous variant A/G snv 0.33 0.34 81
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs7975232
VDR
0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 56
rs1169288
HNF1A-AS1 ; HNF1A
0.776 0.160 12 120978847 missense variant A/C;T snv 0.35 21
rs11053646
OLR1
0.724 0.280 12 10160849 missense variant C/G snv 0.11 0.13 18
rs2464196
HNF1A
0.742 0.320 12 120997624 missense variant G/A snv 0.34 0.27 17
rs7961581
TSPAN8
0.827 0.200 12 71269322 intron variant C/T snv 0.75 7
rs1800574
HNF1A ; HNF1A-AS1
0.882 0.080 12 120979061 missense variant C/T snv 2.9E-02 2.2E-02 6