Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs878854066
TP53
0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs869320673
APPL1
0.882 0.080 3 57260016 stop gained T/A snv 4
rs867232360
GCK
1.000 0.040 7 44145552 missense variant C/T snv 3
rs867120336
KLF11
1.000 0.040 2 10048589 frameshift variant -/A delins 4.1E-06 2
rs864745
JAZF1
0.763 0.320 7 28140937 intron variant T/C snv 0.41 12
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs822396
ADIPOQ
0.732 0.400 3 186849088 intron variant G/A snv 0.81 16
rs8193037
IL17A
0.752 0.320 6 52186311 upstream gene variant G/A;T snv 12
rs8192678
PPARGC1A
0.667 0.440 4 23814039 missense variant C/T snv 0.31 0.26 28
rs8192675
SLC2A2
0.925 0.080 3 171007094 intron variant T/C snv 0.42 5
rs8192284
IL6R
0.724 0.720 1 154454494 missense variant A/C;T snv 19
rs8133052
CBR3 ; CBR3-AS1
0.925 0.120 21 36135203 missense variant G/A;C snv 0.44 6
rs8111699
STK11
0.851 0.200 19 1209715 intron variant C/G snv 0.53 6
rs8099917 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 60
rs8096658
NFATC1 ; LOC107985163
0.925 0.120 18 79396537 intron variant C/G snv 0.39 5
rs8082812 0.851 0.120 18 8522684 intergenic variant C/A snv 4.6E-02 16
rs8065080
TRPV1
0.827 0.200 17 3577153 missense variant T/C snv 0.37 0.32 11
rs8052394
MT1A
0.925 0.080 16 56639916 missense variant A/G snv 0.15 0.14 3
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 32
rs80356664
INS-IGF2 ; INS
0.882 0.120 11 2160878 missense variant C/G;T snv 5
rs80356625
KCNJ11
0.827 0.280 11 17387491 missense variant G/A snv 6
rs80356624
KCNJ11
0.752 0.240 11 17387490 missense variant C/A;T snv 16
rs80356616
KCNJ11
0.732 0.360 11 17387917 missense variant C/T snv 19
rs80356611
KCNJ11
0.790 0.240 11 17387943 missense variant C/A;G;T snv 4.0E-06 10
rs80356610
KCNJ11
0.827 0.080 11 17387968 missense variant A/G snv 6