Disease: Diabetes Mellitus
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs184003
AGER
0.724 0.400 6 32182519 intron variant C/A snv 0.12 0.12 15
rs2070600
AGER
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs237025
SUMO4 ; TAB2
0.672 0.360 6 149400554 missense variant G/A snv 0.55 0.57 26
rs4880
SOD2
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs7756992
CDKAL1
0.827 0.240 6 20679478 intron variant A/G;T snv 12
rs11771443
NOS3
0.790 0.360 7 150990599 upstream gene variant C/T snv 0.16 8
rs16139
NPY ; LOC107986777
0.658 0.560 7 24285260 missense variant T/A;C snv 4.0E-06; 3.0E-02 36
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1800783
NOS3
0.827 0.280 7 150992309 intron variant A/C;G;T snv 7
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1800796
IL6-AS1 ; STEAP1B ; IL6
0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 74
rs2070744
NOS3
0.608 0.680 7 150992991 intron variant C/T snv 0.70 54
rs3918188
NOS3
0.776 0.280 7 151005693 intron variant C/A;T snv 10
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs759853
AKR1B1
0.827 0.320 7 134459206 non coding transcript exon variant G/A snv 0.33 6
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs751141
EPHX2
0.732 0.400 8 27516348 missense variant G/A snv 0.12 0.10 16
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 22
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs4986791
TLR4
0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs5030717
TLR4
0.807 0.240 9 117711556 intron variant A/G snv 0.13 9
rs5030718
TLR4
0.827 0.200 9 117713548 stop gained G/A;T snv 3.1E-03; 8.0E-06 8
rs290487
TCF7L2
0.776 0.280 10 113149972 intron variant C/T snv 0.16 10