Disease: Diabetes Mellitus
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1013773109
GRB14
1.000 0.040 2 164497436 missense variant T/C snv 2.1E-05 2
rs1036915
NTRK2
1.000 0.040 9 84822934 intron variant A/G snv 0.40 2
rs1042488900
ATF6
1.000 0.040 1 161802188 synonymous variant C/T snv 2
rs1042615
AVPR1A
1.000 0.040 12 63150429 missense variant A/C;G;T snv 0.60; 1.2E-05 2
rs10484821
LOC105378024
1.000 0.040 6 139547773 intron variant T/C snv 0.15 2
rs10497721
LOC101927366 ; TMEFF2
1.000 0.040 2 192049636 intron variant C/A;T snv 2
rs1060366
ATP1A1
1.000 0.040 1 116384040 synonymous variant A/G snv 1.3E-03 1.4E-03 2
rs10747983
AVPR1A
1.000 0.040 12 63144678 3 prime UTR variant G/A snv 0.29 2
rs10818684 1.000 0.040 9 122407651 intron variant C/T snv 0.62 2
rs11574
ID3
1.000 0.040 1 23559007 missense variant T/A;C snv 0.80 2
rs1169305
HNF1A
1.000 0.040 12 120999579 missense variant A/G snv 1.00 0.99 2
rs118081497
EEA1
1.000 0.040 12 92782070 missense variant A/T snv 1.1E-02 3.3E-03 2
rs1187274
NTRK2
1.000 0.040 9 84804874 intron variant C/G snv 0.55 2
rs1206634 1.000 0.040 X 96302380 intron variant T/A;G snv 2
rs1236009270
CLEC16A
1.000 0.040 16 10977321 synonymous variant C/T snv 2
rs1240512008
HNF4A
1.000 0.040 20 44413780 missense variant G/A snv 2
rs1260236 1.000 0.040 9 6023030 intergenic variant A/G snv 2
rs1282596664
HNF1B
1.000 0.040 17 37731616 missense variant A/G snv 4.0E-06 2
rs12910524 1.000 0.040 15 101262360 intergenic variant T/A;C snv 2
rs1309065326
TGM2
1.000 0.040 20 38141383 missense variant T/C snv 5.4E-06 7.0E-06 2
rs13427836
HS6ST1
1.000 0.040 2 128270387 intron variant C/T snv 0.11 2
rs1388926124
HNF1A ; HNF1A-AS1
1.000 0.040 12 120978862 missense variant G/A snv 2
rs1406167595
TCF7
1.000 0.040 5 134114958 missense variant G/A snv 1.5E-05 2
rs142318174
HNF1A-AS1 ; HNF1A
1.000 0.040 12 120978923 missense variant G/C snv 2.0E-04 8.1E-04 2
rs143517122
PDX1
1.000 0.040 13 27924267 missense variant G/A;T snv 2.1E-04; 4.2E-06 2