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
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 36
rs7020996 0.925 0.120 9 22129580 downstream gene variant C/A;T snv 3
rs72892910 1.000 0.080 6 50849174 downstream gene variant G/T snv 0.17 2
rs8089364 0.925 0.120 18 60191596 upstream gene variant T/C snv 0.21 6
rs2304130
ZNF101
1.000 0.080 19 19678719 splice region variant A/G snv 0.10 0.12 5
rs11257655 1.000 0.080 10 12265895 TF binding site variant C/T snv 0.23 4
rs7578326
LOC646736
0.882 0.080 2 226155937 TF binding site variant A/G snv 0.36 3
rs11558471
LOC105375716 ; SLC30A8
1.000 0.080 8 117173494 3 prime UTR variant A/G snv 0.25 5
rs3802177
SLC30A8 ; LOC105375716
1.000 0.080 8 117172786 3 prime UTR variant G/A snv 0.24 4
rs6857
NECTIN2
0.790 0.240 19 44888997 3 prime UTR variant C/T snv 0.13 15
rs340874
PROX1 ; PROX1-AS1
0.882 0.080 1 213985913 non coding transcript exon variant T/C snv 0.40 4
rs1800437
GIPR
0.827 0.160 19 45678134 missense variant G/C snv 0.18 0.17 9
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 5
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
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 73
rs5215
KCNJ11
0.827 0.160 11 17387083 missense variant C/T snv 0.64 0.71 3
rs7607980
COBLL1
1.000 0.080 2 164694691 missense variant T/C snv 0.11 0.13 7
rs9891146
C17orf58
1.000 0.080 17 67991933 missense variant T/C snv 0.64 0.60 2
rs5219
KCNJ11
0.701 0.360 11 17388025 stop gained T/A;C snv 0.64 5
rs7173964 1.000 0.080 15 62104743 regulatory region variant G/A snv 0.49 3
rs7374732 1.000 0.080 3 23161963 regulatory region variant C/T snv 0.73 4
rs10795945 1.000 0.080 10 12260608 intergenic variant T/A;C snv 2
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 5
rs12229654 0.763 0.320 12 110976657 intergenic variant T/G snv 4.8E-03 14