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
rs9368222
CDKAL1
1.000 0.080 6 20686765 intron variant C/A;T snv 8
rs2206734
CDKAL1
0.882 0.160 6 20694653 intron variant C/T snv 0.20 4
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 20
rs340874
PROX1 ; PROX1-AS1
0.882 0.080 1 213985913 non coding transcript exon variant T/C snv 0.40 4
rs7020996 0.925 0.120 9 22129580 downstream gene variant C/A;T snv 3
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 5
rs7578326
LOC646736
0.882 0.080 2 226155937 TF binding site variant A/G snv 0.36 3
rs2943634 0.763 0.200 2 226203364 intergenic variant A/C;G snv 8
rs7374732 1.000 0.080 3 23161963 regulatory region variant C/T snv 0.73 4
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 43
rs2237892
KCNQ1
0.790 0.320 11 2818521 intron variant C/T snv 9.2E-02 5
rs2237897
KCNQ1
0.882 0.200 11 2837316 intron variant C/T snv 8.1E-02 3
rs11651052
HNF1B
0.851 0.200 17 37742390 intron variant G/A snv 0.50 7
rs2296172
MACF1
1.000 0.080 1 39370145 missense variant A/G;T snv 0.19; 8.0E-06 4
rs76895963
CCND2-AS1 ; CCND2
1.000 0.080 12 4275678 intron variant T/G snv 1.5E-02 6
rs7034200
GLIS3
1.000 0.080 9 4289050 intron variant C/A;G snv 3
rs6857
NECTIN2
0.790 0.240 19 44888997 3 prime UTR variant C/T snv 0.13 15
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 36
rs11671664
GIPR
0.925 0.120 19 45669020 intron variant G/A snv 0.12 4
rs1800437
GIPR
0.827 0.160 19 45678134 missense variant G/C snv 0.18 0.17 9
rs72892910 1.000 0.080 6 50849174 downstream gene variant G/T snv 0.17 2
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31 16
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 11
rs7193144
FTO
0.925 0.120 16 53776774 intron variant T/C snv 0.40 5
rs8043757
FTO
0.925 0.120 16 53779538 intron variant A/T snv 0.40 5