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
rs9989419 0.882 0.120 16 56951227 regulatory region variant A/G snv 0.55 11
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs870992
ITGA1
1.000 0.080 5 52897406 intron variant A/G snv 7.9E-02 7.0E-02 3
rs855791
TMPRSS6
0.701 0.400 22 37066896 missense variant A/G;T snv 0.57; 4.0E-06 38
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs7570971
RAB3GAP1
1.000 0.080 2 135080336 intron variant C/A snv 0.61 5
rs7412
APOE
0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 47
rs688
LDLR
0.742 0.400 19 11116926 synonymous variant C/T snv 0.39 0.34 16
rs6857
NECTIN2
0.790 0.240 19 44888997 3 prime UTR variant C/T snv 0.13 16
rs679899
APOB
0.925 0.080 2 21028042 missense variant G/A snv 0.49 0.39 7
rs651007 0.851 0.160 9 133278431 upstream gene variant T/A;C snv 22
rs649129 1.000 0.080 9 133278860 upstream gene variant T/C;G snv 10
rs635634 0.882 0.160 9 133279427 upstream gene variant T/A;C snv 22
rs599839
PSRC1
0.724 0.360 1 109279544 downstream gene variant G/A;C snv 27
rs58542926
TM6SF2
0.630 0.440 19 19268740 missense variant C/T snv 6.5E-02 5.8E-02 42
rs579459 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 28
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 21
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 24
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43
rs429358
APOE
0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 66
rs405509
APOE
0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58 30
rs3817588
GCKR
0.882 0.160 2 27508345 intron variant T/C snv 0.14 7
rs3794991
GATAD2A
1.000 0.080 19 19499787 intron variant C/G;T snv 7.4E-02 5
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 26
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92