Disease: Diabetes Mellitus, Non-Insulin-Dependent
Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10795945 1.000 0.080 10 12260608 intergenic variant T/A;C snv 2
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 11
rs12454712
BCL2
0.925 0.120 18 63178651 intron variant T/A;C snv 7
rs2246012
ARG1 ; MED23
1.000 0.080 6 131577068 intron variant T/A;C snv 2
rs2296172
MACF1
1.000 0.080 1 39370145 missense variant A/G;T snv 0.19; 8.0E-06 4
rs2307111
POC5
0.925 0.120 5 75707853 missense variant T/A;C snv 4.5E-06; 0.47 5
rs2943634 0.763 0.200 2 226203364 intergenic variant A/C;G snv 8
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 73
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv 19
rs5219
KCNJ11
0.701 0.360 11 17388025 stop gained T/A;C snv 0.64 5
rs7020996 0.925 0.120 9 22129580 downstream gene variant C/A;T snv 3
rs7034200
GLIS3
1.000 0.080 9 4289050 intron variant C/A;G snv 3
rs7185735
FTO
0.925 0.120 16 53788739 intron variant A/G;T snv 5
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 19
rs7923837 0.882 0.160 10 92722160 intergenic variant G/A;T snv 3
rs9368222
CDKAL1
1.000 0.080 6 20686765 intron variant C/A;T snv 8
rs12229654 0.763 0.320 12 110976657 intergenic variant T/G snv 4.8E-03 14
rs76895963
CCND2-AS1 ; CCND2
1.000 0.080 12 4275678 intron variant T/G snv 1.5E-02 6
rs2237897
KCNQ1
0.882 0.200 11 2837316 intron variant C/T snv 8.1E-02 3
rs11709077
PPARG
0.925 0.120 3 12295008 intron variant G/A snv 8.8E-02 3
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 5
rs2237892
KCNQ1
0.790 0.320 11 2818521 intron variant C/T snv 9.2E-02 5
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 23
rs11671664
GIPR
0.925 0.120 19 45669020 intron variant G/A snv 0.12 4
rs2304130
ZNF101
1.000 0.080 19 19678719 splice region variant A/G snv 0.10 0.12 5