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
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs726344
FNDC5
0.882 0.120 1 32867503 intron variant G/A snv 0.16 3
rs7538490
NOS1AP ; LOC105371475
0.925 0.120 1 162121540 intron variant T/C snv 0.70 2
rs80356814
LMNA
0.732 0.320 1 156138697 synonymous variant C/T snv 8.0E-06 15
rs12104705
KCNH7
0.882 0.120 2 162435107 intron variant C/T snv 0.15 4
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs1801278
IRS1
0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02 38
rs183433761
GCG ; LOC101929532
0.851 0.200 2 162152278 5 prime UTR variant T/C;G snv 5
rs1968482
ADCY3
0.925 0.120 2 24863989 intron variant T/C snv 0.32 2
rs2118404
EFR3B
0.925 0.120 2 25154460 3 prime UTR variant C/A;G;T snv 2
rs2302870
KLF7
0.925 0.120 2 207088682 intron variant T/C;G snv 2
rs2867125 0.925 0.120 2 622827 intergenic variant T/A;C snv 0.85 8
rs2943641 0.763 0.160 2 226229029 intergenic variant T/C snv 0.67 18
rs3923113 0.882 0.120 2 164645339 intergenic variant A/C;G;T snv 3
rs4988235
MCM6
0.752 0.400 2 135851076 intron variant G/A;C snv 19
rs6749704
CCL20
0.827 0.240 2 227813126 intron variant T/C snv 0.24 5
rs7561317 0.925 0.120 2 644953 intergenic variant A/G snv 0.81 7
rs7568369
KLF7 ; MIR7845 ; MYOSLID
0.925 0.120 2 207166591 intron variant G/T snv 0.38 2
rs7578597
THADA
0.807 0.240 2 43505684 missense variant T/C snv 9.9E-02 0.14 7
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs8192673
GRB14
0.925 0.120 2 164497202 intron variant C/A;T snv 4.0E-06; 0.67 2
rs1052133
OGG1 ; CAMK1
0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs13078807
CADM2
0.925 0.120 3 85835000 intron variant A/G snv 0.15 5
rs1501299
ADIPOQ ; ADIPOQ-AS1
0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs16861194
ADIPOQ
0.925 0.120 3 186841636 upstream gene variant A/G snv 0.15 2