Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2568958
LOC105378797
0.882 0.160 1 72299433 intron variant G/A;C snv 8
rs34811474
ANAPC4
1.000 0.040 4 25407216 missense variant G/A;T snv 0.15; 4.1E-06 8
rs4607517
GCK
0.882 0.080 7 44196069 intron variant G/A;C snv 8
rs7923837 0.882 0.160 10 92722160 intergenic variant G/A;T snv 8
rs9368222
CDKAL1
1.000 0.080 6 20686765 intron variant C/A;T snv 8
rs1053874
DNASE1 ; TRAP1
0.851 0.240 16 3657746 missense variant G/A;T snv 0.36; 4.0E-06 7
rs13130484 1.000 0.080 4 45173674 intergenic variant C/A;T snv 7
rs17630235
TRAFD1
0.925 0.120 12 112153882 downstream gene variant G/A;C snv 7
rs9930333
FTO
0.882 0.120 16 53766065 intron variant T/C;G snv 7
rs12513649 0.851 0.160 5 173045049 regulatory region variant C/G;T snv 6
rs72681869
SOS2
14 50188639 missense variant G/A;C snv 4.0E-06; 4.1E-03 6
rs7740107
L3MBTL3
1.000 0.080 6 130053316 intron variant T/A;G snv 6
rs887912 1.000 0.080 2 59075742 intron variant T/C;G snv 6
rs11658063
HNF1B
0.851 0.120 17 37743881 intron variant G/C;T snv 5
rs12140153
PATJ
1 62114219 missense variant G/A;T snv 4.0E-06; 5.9E-02 5
rs1884897 20 6632185 regulatory region variant A/G;T snv 5
rs2307111
POC5
0.925 0.120 5 75707853 missense variant T/A;C snv 4.5E-06; 0.47 5
rs4836133
LOC105379158 ; LINC02240
0.925 0.160 5 124996410 intron variant C/A;G;T snv 5
rs7185735
FTO
0.925 0.120 16 53788739 intron variant A/G;T snv 5
rs72755233
ADAMTS17
1.000 0.080 15 100152748 missense variant G/A;T snv 7.1E-02; 3.2E-05 5
rs8049439
ATXN2L
0.925 0.120 16 28826194 intron variant T/C;G snv 0.38 5
rs10458787 1.000 0.040 10 4613373 intergenic variant A/C;G snv 4
rs12286929 0.925 0.080 11 115151684 intergenic variant A/C;G snv 4
rs12463617 1.000 0.080 2 629244 regulatory region variant A/C;T snv 4
rs177430
NPC1 ; RMC1
18 23506161 intron variant C/A;T snv 4