Disease: Diabetes Mellitus, Non-Insulin-Dependent
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1801278
IRS1
0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02 38
rs1805094
LEPR
0.716 0.440 1 65610269 missense variant G/C;T snv 0.16; 4.0E-06 16
rs1805097
IRS2
0.689 0.360 13 109782884 missense variant C/G;T snv 0.35 22
rs1805192
PPARG
0.510 0.840 3 12379739 missense variant C/G snv 121
rs183433761
GCG ; LOC101929532
0.851 0.200 2 162152278 5 prime UTR variant T/C;G snv 5
rs201777403
ADRB2
0.925 0.120 5 148827105 missense variant G/A snv 4.0E-06 2
rs2118404
EFR3B
0.925 0.120 2 25154460 3 prime UTR variant C/A;G;T snv 2
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 57
rs2231142
ABCG2
0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 56
rs2237895
KCNQ1
0.790 0.240 11 2835964 intron variant A/C;T snv 10
rs2241766
ADIPOQ ; ADIPOQ-AS1
0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48
rs225011
DIO2
0.925 0.120 14 80205865 intron variant T/A;C snv 2
rs2274907
ITLN1
0.851 0.200 1 160882036 missense variant A/G;T snv 0.66 5
rs2295490
TRIB3
0.724 0.320 20 388261 missense variant A/G;T snv 0.18; 4.0E-06 16
rs2297508
SREBF1
0.790 0.240 17 17812003 synonymous variant C/G;T snv 0.50; 7.5E-05 8
rs2302870
KLF7
0.925 0.120 2 207088682 intron variant T/C;G snv 2
rs2307111
POC5
0.925 0.120 5 75707853 missense variant T/A;C snv 4.5E-06; 0.47 5
rs2514259
AIP
0.807 0.280 11 67479201 upstream gene variant C/G;T snv 8
rs2568958
LOC105378797
0.882 0.160 1 72299433 intron variant G/A;C snv 8
rs266729
ADIPOQ
0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs3135506
APOA5
0.708 0.400 11 116791691 missense variant G/A;C snv 3.0E-05; 6.8E-02 26
rs35518301
HBD
0.827 0.200 11 5234514 5 prime UTR variant T/C snv 6
rs35767
IGF1 ; LOC105369944
0.763 0.360 12 102481791 upstream gene variant A/C;G;T snv 13
rs361072
PIK3CB
0.882 0.120 3 138759702 intron variant G/A;C snv 4
rs3813929
HTR2C
0.851 0.240 X 114584047 upstream gene variant C/G;T snv 5