Disease: Diabetes Mellitus
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10757283 0.827 0.120 9 22134173 intergenic variant C/A;T snv 0.45 6
rs10761600
ARID5B
0.925 0.120 10 61997361 intron variant A/G;T snv 3
rs10767664
BDNF
0.752 0.400 11 27704439 intron variant T/A snv 0.83 16
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 22
rs10830963
MTNR1B
0.776 0.400 11 92975544 intron variant C/G snv 0.22 27
rs10885390 0.925 0.080 10 112881038 regulatory region variant T/A snv 0.30 3
rs10911021
LOC105371642 ; LINC01344
0.807 0.160 1 182112825 intron variant C/T snv 0.36 11
rs10946398
CDKAL1
0.827 0.160 6 20660803 intron variant A/C snv 0.40 7
rs11066280
HECTD4
0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 27
rs11196205
TCF7L2
0.827 0.200 10 113047288 intron variant G/A;C;T snv 7
rs11212617
C11orf65
0.827 0.200 11 108412434 intron variant C/A snv 0.49 7
rs1137933
NOS2
0.882 0.160 17 27778906 synonymous variant G/A snv 0.20 0.21 4
rs114202595
PAX4
0.882 0.120 7 127614533 missense variant G/A;T snv 1.2E-04; 9.1E-06 4
rs11549465
HIF1A-AS3 ; HIF1A
0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02 55
rs11614913
HOXC6 ; MIR196A2
0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs1169288
HNF1A-AS1 ; HNF1A
0.776 0.160 12 120978847 missense variant A/C;T snv 0.35 21
rs11771443
NOS3
0.790 0.360 7 150990599 upstream gene variant C/T snv 0.16 8
rs1181860747
INSR
0.776 0.240 19 7122961 missense variant C/T snv 10
rs11864909
PDILT
0.851 0.160 16 20389517 intron variant C/T snv 0.23 7
rs11868035
RAI1 ; SREBF1
0.763 0.200 17 17811787 splice region variant G/A snv 0.45 0.33 14
rs1188383936
F2
0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 102
rs12026
PON2
0.827 0.240 7 95411704 missense variant G/C snv 0.27 0.27 6
rs12104705
KCNH7
0.882 0.120 2 162435107 intron variant C/T snv 0.15 4
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs121908279
INS ; INS-IGF2
0.925 0.080 11 2159983 missense variant G/T snv 2.5E-05 2.1E-05 3