Disease: Diabetes Mellitus, Non-Insulin-Dependent
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10146997
NRXN3
0.827 0.240 14 79478819 intron variant A/G snv 0.25 6
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 25
rs10423928
GIPR
0.807 0.200 19 45679046 intron variant T/A snv 0.19 12
rs1043307
PSMD9
0.776 0.360 12 121915890 missense variant A/C;G snv 14
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
rs10885406
TCF7L2
0.925 0.120 10 113017965 intron variant A/G snv 0.55 2
rs10895068
PGR ; PGR-AS1
0.752 0.240 11 101129483 5 prime UTR variant C/T snv 3.6E-02 14
rs10911021
LOC105371642 ; LINC01344
0.807 0.160 1 182112825 intron variant C/T snv 0.36 11
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 19
rs10946398
CDKAL1
0.827 0.160 6 20660803 intron variant A/C snv 0.40 7
rs10968576
LINGO2
0.882 0.120 9 28414341 intron variant A/G snv 0.26 10
rs11075989
FTO
0.925 0.120 16 53785965 intron variant C/A;T snv 3
rs11075990
FTO
0.925 0.120 16 53785981 intron variant A/G snv 0.41 6
rs11076023
FTO
0.925 0.120 16 54118136 3 prime UTR variant A/T snv 0.49 2
rs11196205
TCF7L2
0.827 0.200 10 113047288 intron variant G/A;C;T snv 7
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 18
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs11642015
FTO
0.925 0.120 16 53768582 intron variant C/T snv 0.31 9
rs11642841
FTO
0.925 0.120 16 53811575 intron variant C/A;G snv 3
rs11671664
GIPR
0.925 0.120 19 45669020 intron variant G/A snv 0.12 5
rs1181860747
INSR
0.776 0.240 19 7122961 missense variant C/T snv 10
rs12104705
KCNH7
0.882 0.120 2 162435107 intron variant C/T snv 0.15 4
rs12156368
PSD3
0.925 0.120 8 18885203 intron variant C/T snv 0.36 2