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
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
rs104894014
GCK
0.925 0.080 7 44145167 missense variant G/A snv 2
rs10517086
LINC02357
0.882 0.160 4 26083889 intron variant G/A snv 0.27 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
rs11071657 1.000 0.040 15 62141763 regulatory region variant A/G snv 0.31 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
rs11920090
SLC2A2
1.000 0.040 3 170999732 intron variant T/A snv 0.20 2
rs1206634 1.000 0.040 X 96302380 intron variant T/A;G snv 2
rs12144939
CFH
0.925 0.080 1 196729815 intron variant G/A;T snv 2
rs121917718
PAX4
0.925 0.080 7 127613804 missense variant G/A snv 5.2E-05 3.5E-05 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