Disease: Diabetes Mellitus
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1036483919
GCK
0.925 0.080 7 44151050 missense variant A/G snv 4.0E-06 4
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1042714
ADRB2
0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs1044498
ENPP1
0.752 0.360 6 131851228 missense variant A/C;G snv 0.19 15
rs1057520504
HNF1A
0.882 0.080 12 120994238 missense variant G/A snv 4
rs1063856
VWF
0.763 0.400 12 6044368 missense variant T/C;G snv 0.31 14
rs10761600
ARID5B
0.925 0.120 10 61997361 intron variant A/G;T snv 3
rs11196205
TCF7L2
0.827 0.200 10 113047288 intron variant G/A;C;T snv 7
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs114202595
PAX4
0.882 0.120 7 127614533 missense variant G/A;T snv 1.2E-04; 9.1E-06 4
rs1169288
HNF1A-AS1 ; HNF1A
0.776 0.160 12 120978847 missense variant A/C;T snv 0.35 21
rs1181860747
INSR
0.776 0.240 19 7122961 missense variant C/T snv 10
rs1188383936
F2
0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 102
rs121909244
PPARG
0.776 0.160 3 12434111 missense variant C/A;T snv 4.0E-06 11
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
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
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs1275561861
HLA-A
0.672 0.360 6 29944350 missense variant G/A snv 23
rs12785878
NADSYN1
0.677 0.520 11 71456403 intron variant G/A;T snv 25
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
rs1337503417
KRT16
0.790 0.160 17 41612325 missense variant G/T snv 4.0E-06 12