Disease: Diabetes Mellitus
Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10116772
GLIS3
0.882 0.080 9 4290541 intron variant C/A;T snv 2
rs1036483919
GCK
0.925 0.080 7 44151050 missense variant A/G snv 4.0E-06 4
rs1042488900
ATF6
1.000 0.040 1 161802188 synonymous variant C/T snv 2
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1042615
AVPR1A
1.000 0.040 12 63150429 missense variant A/C;G;T snv 0.60; 1.2E-05 2
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
rs10489177
C1orf112 ; METTL18
0.925 0.120 1 169793666 missense variant T/A;G snv 4.1E-06; 0.19 4
rs104894014
GCK
0.925 0.080 7 44145167 missense variant G/A snv 2
rs1056534
FN3K ; TBCD
0.882 0.200 17 82750725 synonymous variant C/A;G;T snv 0.62 5
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 11
rs10887800
LOC101929727 ; RNLS
0.790 0.280 10 88316086 intron variant A/G;T snv 11
rs11196205
TCF7L2
0.827 0.200 10 113047288 intron variant G/A;C;T snv 7
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 11
rs1129844
CCL11
0.752 0.320 17 34285875 missense variant G/A;C;T snv 0.16; 1.2E-05 13
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 213
rs114202595
PAX4
0.882 0.120 7 127614533 missense variant G/A;T snv 1.2E-04; 9.1E-06 4
rs11547328
CDK4
0.701 0.360 12 57751648 missense variant G/A;T snv 4.0E-06 22
rs11574
ID3
1.000 0.040 1 23559007 missense variant T/A;C snv 0.80 2
rs11575937
LMNA
0.653 0.480 1 156136985 missense variant G/A;T snv 15
rs11672433
ANGPTL4
0.925 0.120 19 8373832 synonymous variant G/A;C snv 0.10; 4.0E-06 3
rs1169288
HNF1A-AS1 ; HNF1A
0.776 0.160 12 120978847 missense variant A/C;T snv 0.35 12
rs1188383936
F2
0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 102
rs1206634 1.000 0.040 X 96302380 intron variant T/A;G snv 2