Disease: Diabetes Mellitus, Insulin-Dependent
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 22
rs1358030 0.925 0.120 10 106363841 intergenic variant G/A snv 0.57 2
rs7111341 0.925 0.120 11 2191936 regulatory region variant C/T snv 0.29 2
rs71597855 0.807 0.240 4 53790270 intron variant G/A snv 2.5E-02 7
rs7202877 0.882 0.160 16 75213347 intergenic variant T/C;G snv 3
rs1205538057
ACE
0.827 0.200 17 63483937 missense variant A/G snv 4.0E-06 5
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs762890235
ACE2
0.827 0.240 X 15578220 missense variant G/T snv 3.8E-05 9.5E-06 5
rs17300539
ADIPOQ
0.752 0.320 3 186841671 upstream gene variant G/A snv 5.3E-02 11
rs266729
ADIPOQ
0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs1042713
ADRB2
0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs2070600
AGER
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs4762
AGT
0.637 0.440 1 230710231 missense variant G/A snv 0.12 0.11 35
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs759853
AKR1B1
0.827 0.320 7 134459206 non coding transcript exon variant G/A snv 0.33 6
rs1332629192
ALB
0.851 0.200 4 73404374 missense variant C/T snv 7
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs1001179
CAT
0.641 0.680 11 34438684 upstream gene variant C/T snv 0.16 33
rs769217
CAT
0.742 0.440 11 34461361 synonymous variant C/T snv 0.25 0.22 12
rs5443
CDCA3 ; GNB3
0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs231775
CTLA4
0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs5742909
CTLA4
0.614 0.680 2 203867624 upstream gene variant C/T snv 6.7E-02 40
rs4673
CYBA
0.653 0.600 16 88646828 missense variant A/G;T snv 0.70 32
rs10741657
CYP2R1
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 34
rs12794714
CYP2R1
0.708 0.360 11 14892029 synonymous variant G/A snv 0.41 0.35 15