Disease: Diabetes Mellitus
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs10911021
LOC105371642 ; LINC01344
0.807 0.160 1 182112825 intron variant C/T snv 0.36 11
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1805094
LEPR
0.716 0.440 1 65610269 missense variant G/C;T snv 0.16; 4.0E-06 16
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 57
rs35439639
AVPR1B
1.000 0.080 1 206109537 3 prime UTR variant C/G;T snv 2
rs35608965
AVPR1B
1.000 0.080 1 206116919 5 prime UTR variant A/G snv 4.9E-02 6.2E-02 2
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs4762
AGT
0.637 0.440 1 230710231 missense variant G/A snv 0.12 0.11 35
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
rs5744168
TLR5
0.701 0.480 1 223111858 stop gained G/A snv 5.3E-02 4.4E-02 18
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs7211
TXNIP
0.827 0.200 1 145993449 3 prime UTR variant G/A;C;T snv 6
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
rs1269801977
PPIG
0.925 0.120 2 169604087 missense variant A/G snv 4.0E-06 7.0E-06 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
rs561017686
NEUROD1 ; CERKL
0.882 0.120 2 181678138 missense variant G/A;C snv 8.0E-06; 8.4E-04 4
rs6548238 0.882 0.200 2 634905 TF binding site variant T/C snv 0.85 10
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
rs1052133
OGG1 ; CAMK1
0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147