Disease: Diabetes Mellitus
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121909244
PPARG
0.776 0.160 3 12434111 missense variant C/A;T snv 4.0E-06 11
rs121912645
KLF11
0.882 0.080 2 10048376 missense variant G/T snv 1.3E-04 8.4E-05 4
rs12229654 0.763 0.320 12 110976657 intergenic variant T/G snv 4.8E-03 20
rs12255372
TCF7L2
0.667 0.480 10 113049143 intron variant G/A;T snv 28
rs1232898090
PPARA
0.637 0.600 22 46198429 missense variant G/C;T snv 4.0E-06; 4.0E-06 40
rs12363572 0.925 0.080 11 68621498 upstream gene variant C/T snv 0.10 3
rs1241356540
ACE
0.851 0.160 17 63497137 missense variant C/T snv 5
rs12513649 0.851 0.160 5 173045049 regulatory region variant C/G;T snv 6
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs1272388614
ABCC8
0.851 0.080 11 17395658 missense variant C/T snv 2.4E-05 3.5E-05 5
rs1275561861
HLA-A
0.672 0.360 6 29944350 missense variant G/A snv 23
rs12779790 0.882 0.120 10 12286011 intergenic variant A/G snv 0.17 5
rs12785878
NADSYN1
0.677 0.520 11 71456403 intron variant G/A;T snv 25
rs12917707
UMOD
0.827 0.200 16 20356368 upstream gene variant G/T snv 0.14 11
rs12979860
IFNL4
0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs12980275 0.701 0.360 19 39241143 upstream gene variant A/G snv 0.36 23
rs1308346790
RBPJ
0.925 0.080 4 26430444 missense variant T/C snv 4.0E-06 3
rs13266634
SLC30A8 ; LOC105375716
0.724 0.480 8 117172544 missense variant C/A;T snv 0.29 23
rs1332629192
ALB
0.851 0.200 4 73404374 missense variant C/T snv 7
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs13333226
UMOD
0.827 0.200 16 20354332 intron variant A/G snv 0.23 10
rs1337503417
KRT16
0.790 0.160 17 41612325 missense variant G/T snv 4.0E-06 12
rs1364181648
SHOC1
0.925 0.080 9 111738418 missense variant A/G snv 8.0E-06 3
rs137852783
PDX1
0.882 0.080 13 27920364 missense variant G/A;T snv 2.9E-03 4