Disease: Diabetes Mellitus
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5068
NPPA ; NPPA-AS1 ; CLCN6
0.776 0.160 1 11845917 3 prime UTR variant A/G;T snv 13
rs5082
APOA2
0.807 0.160 1 161223893 upstream gene variant G/A snv 0.68 8
rs5275
PTGS2
0.583 0.560 1 186673926 3 prime UTR variant A/G;T snv 55
rs5361
SELE ; C1orf112
0.623 0.720 1 169731919 missense variant T/G snv 8.3E-02; 8.0E-06 7.8E-02 47
rs536289169
GSTM1 ; GSTM2
0.752 0.360 1 109688180 missense variant C/T snv 4.8E-04 13
rs5744168
TLR5
0.701 0.480 1 223111858 stop gained G/A snv 5.3E-02 4.4E-02 18
rs60662302
LMNA
0.882 0.200 1 156138593 missense variant G/A snv 2.1E-04 7.7E-04 5
rs6136
SELP
0.752 0.440 1 169594713 missense variant T/G snv 8.2E-02 7.5E-02 17
rs6681231 0.882 0.120 1 186690727 intergenic variant G/C snv 0.22 5
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs7212
TXNIP
0.851 0.120 1 145992816 3 prime UTR variant G/C snv 0.16 5
rs751377893
F5
0.574 0.680 1 169546513 missense variant T/C snv 4.0E-06 65
rs1037733674
GCG ; LOC101929532
0.882 0.120 2 162147429 missense variant T/C snv 1.4E-05 5
rs12104705
KCNH7
0.882 0.120 2 162435107 intron variant C/T snv 0.15 4
rs121912645
KLF11
0.882 0.080 2 10048376 missense variant G/T snv 1.3E-04 8.4E-05 4
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs16944
IL1B
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs1801262
NEUROD1 ; CERKL
0.882 0.120 2 181678728 missense variant T/C snv 0.70 0.68 4
rs1801278
IRS1
0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02 38
rs2943641 0.763 0.160 2 226229029 intergenic variant T/C snv 0.67 18
rs34336420
KLF11
0.882 0.080 2 10047996 missense variant C/G;T snv 4.0E-06; 3.3E-03 4
rs35927125
KLF11
0.925 0.080 2 10046292 missense variant A/G;T snv 9.3E-02 3
rs560887
SPC25 ; G6PC2
0.827 0.120 2 168906638 intron variant T/C snv 0.79 0.80 18
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 21
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 59