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
rs10224002
PRKAG2
0.925 0.080 7 151717955 intron variant A/G snv 0.31 12
rs11097432
PDLIM5
1.000 0.080 4 94658554 intron variant T/C snv 0.24 2
rs12576239
KCNQ1
1.000 0.080 11 2481089 intron variant C/T snv 0.16 3
rs13306519
LEPR
1.000 0.080 1 65572246 intron variant C/G;T snv 2
rs137853240
HNF1A
0.807 0.080 12 120994405 missense variant G/A snv 1.4E-05 8
rs2272592
DDAH2 ; CLIC1
1.000 0.080 6 31730575 5 prime UTR variant T/C snv 0.88 2
rs3762344
LOC105372879
1.000 0.080 1 206895327 upstream gene variant G/A snv 0.47 2
rs3864884
KCNQ1
1.000 0.080 11 2460862 intron variant C/T snv 0.30 2
rs75843691
EPHA4
1.000 0.080 2 221530901 intron variant C/A;G;T snv 2
rs76974938
CFAP298-TCP10L ; CFAP298
1.000 0.080 21 32609946 missense variant C/T snv 1.3E-04 5.5E-04 3
rs7770619
PPARD
1.000 0.080 6 35382265 intron variant C/T snv 7.7E-02 2
rs1037733674
GCG ; LOC101929532
0.882 0.120 2 162147429 missense variant T/C snv 1.4E-05 5
rs1150256
IL24
0.925 0.120 1 206899788 intron variant G/A snv 0.40 4
rs1558902
FTO
0.827 0.120 16 53769662 intron variant T/A snv 0.31 21
rs1805081
NPC1
0.925 0.120 18 23560468 missense variant T/C snv 0.33 0.29 3
rs2070895
LIPC ; ALDH1A2
0.807 0.120 15 58431740 intron variant G/A snv 0.33 15
rs4646188
ACE2
0.925 0.120 X 15583220 intron variant A/G snv 9.1E-02 4
rs4757268
PDE3B
0.827 0.120 11 14789216 synonymous variant A/G snv 0.63 0.64 6
rs9817428
PPARG
0.925 0.120 3 12298768 intron variant C/A snv 0.31 3
rs9838915
KLF15
0.882 0.120 3 126347377 intron variant G/A snv 0.19 4
rs11572080
CYP2C8
0.882 0.160 10 95067273 missense variant C/A;T snv 8.3E-02 4
rs121909244
PPARG
0.776 0.160 3 12434111 missense variant C/A;T snv 4.0E-06 11
rs1337503417
KRT16
0.790 0.160 17 41612325 missense variant G/T snv 4.0E-06 12
rs1372503923
ITGA2
0.925 0.160 5 53048731 missense variant A/C snv 3
rs146052672
HMGA1
0.851 0.160 6 34242693 intron variant -/C delins 5