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
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs429358
APOE
0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 66
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 57
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv 34
rs405509
APOE
0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58 30
rs579459 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 28
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 25
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 24
rs651007 0.851 0.160 9 133278431 upstream gene variant T/A;C snv 22
rs1169288
HNF1A-AS1 ; HNF1A
0.776 0.160 12 120978847 missense variant A/C;T snv 0.35 21
rs1558902
FTO
0.827 0.120 16 53769662 intron variant T/A snv 0.31 21
rs1800961
HNF4A
0.851 0.160 20 44413724 missense variant C/T snv 3.1E-02 2.5E-02 21
rs687621
ABO
0.851 0.240 9 133261662 intron variant G/A;C snv 18
rs2464196
HNF1A
0.742 0.320 12 120997624 missense variant G/A snv 0.34 0.27 17
rs6857
NECTIN2
0.790 0.240 19 44888997 3 prime UTR variant C/T snv 0.13 16
rs3093059
CRP
0.752 0.520 1 159715346 upstream gene variant A/G snv 0.13 11
rs649129 1.000 0.080 9 133278860 upstream gene variant T/C;G snv 10
rs3093077 0.827 0.200 1 159709846 upstream gene variant A/C;G;T snv 9
rs6700896
LEPR
0.827 0.160 1 65624099 intron variant C/T snv 0.44 9
rs2393791
HNF1A
0.925 0.160 12 120986153 intron variant C/T snv 0.62 8
rs1892534
LEPR
0.925 0.120 1 65640261 3 prime UTR variant C/T snv 0.44 7
rs3817588
GCKR
0.882 0.160 2 27508345 intron variant T/C snv 0.14 7
rs7310409
HNF1A
0.925 0.160 12 120987058 intron variant A/C;G;T snv 7