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
rs6857
NECTIN2
0.790 0.240 19 44888997 3 prime UTR variant C/T snv 0.13 15
rs7607980
COBLL1
1.000 0.080 2 164694691 missense variant T/C snv 0.11 0.13 7
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 5
rs72892910 1.000 0.080 6 50849174 downstream gene variant G/T snv 0.17 2
rs1800437
GIPR
0.827 0.160 19 45678134 missense variant G/C snv 0.18 0.17 9
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 36
rs11708067
ADCY5
0.882 0.080 3 123346931 intron variant A/G snv 0.19 6
rs6947395
AUTS2
1.000 0.080 7 69941675 intron variant A/T snv 0.20 2
rs2206734
CDKAL1
0.882 0.160 6 20694653 intron variant C/T snv 0.20 4
rs12970134 0.790 0.280 18 60217517 intergenic variant G/A snv 0.21 7
rs8089364 0.925 0.120 18 60191596 upstream gene variant T/C snv 0.21 6
rs7144011
NRXN3
1.000 0.080 14 79474040 intron variant G/T snv 0.21 4
rs10830963
MTNR1B
0.776 0.400 11 92975544 intron variant C/G snv 0.22 10
rs11257655 1.000 0.080 10 12265895 TF binding site variant C/T snv 0.23 4
rs3802177
SLC30A8 ; LOC105375716
1.000 0.080 8 117172786 3 prime UTR variant G/A snv 0.24 4
rs11558471
LOC105375716 ; SLC30A8
1.000 0.080 8 117173494 3 prime UTR variant A/G snv 0.25 5
rs35261542
CDKAL1
1.000 0.080 6 20675561 intron variant C/A snv 0.26 3
rs1899951
PPARG
0.851 0.160 3 12353341 intron variant C/T snv 0.26 2
rs3751812
FTO
0.882 0.160 16 53784548 intron variant G/T snv 0.30 7
rs17817964
FTO
0.925 0.120 16 53794154 intron variant C/T snv 0.30 6
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31 16
rs7578326
LOC646736
0.882 0.080 2 226155937 TF binding site variant A/G snv 0.36 3
rs8043757
FTO
0.925 0.120 16 53779538 intron variant A/T snv 0.40 5
rs7193144
FTO
0.925 0.120 16 53776774 intron variant T/C snv 0.40 5
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 16