Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 45
rs780093
GCKR
0.763 0.240 2 27519736 intron variant T/C snv 0.68 30
rs1800588
ALDH1A2 ; LIPC
0.790 0.200 15 58431476 intron variant C/G;T snv 0.30 16
rs4580704
CLOCK
0.790 0.200 4 55460540 intron variant G/C snv 0.69 13
rs11932595
CLOCK
0.827 0.160 4 55457430 intron variant A/G;T snv 12
rs4845625
IL6R
0.851 0.080 1 154449591 intron variant T/C snv 0.60 9
rs57137919
ABCG1 ; LOC105372814
0.776 0.160 21 42218908 intron variant G/A snv 0.14 9
rs2393791
HNF1A
0.925 0.160 12 120986153 intron variant C/T snv 0.62 8
rs10790162
BUD13
0.882 0.160 11 116768388 intron variant A/G;T snv 0.93 7
rs10808546 8 125483576 intron variant C/T snv 0.39 7
rs17514846
FURIN
0.882 0.120 15 90873320 intron variant C/A;G snv 7
rs7310409
HNF1A
0.925 0.160 12 120987058 intron variant A/C;G;T snv 7
rs7973260
KSR2
0.851 0.120 12 117937681 intron variant A/G snv 0.83 7
rs1168013
DOCK7
1.000 0.120 1 62531167 intron variant C/G;T snv 6
rs1169313
C12orf43
12 121004867 intron variant T/A;C snv 6
rs6782181
MRAS
0.851 0.160 3 138386212 intron variant G/A;C snv 6
rs6982502 0.882 0.080 8 125467120 intron variant C/T snv 0.62 6
rs2569512
ILF3
0.925 0.080 19 10679486 intron variant T/C snv 0.76 5
rs3828599
GPX3 ; LOC105378228
0.882 0.040 5 151022235 intron variant A/G snv 0.67 5
rs5072
APOA1 ; APOA1-AS
11 116836867 intron variant A/G snv 0.89 5
rs11206517
PCSK9
1.000 0.120 1 55060755 intron variant T/C;G snv 4
rs11773845
CAV1
0.925 0.120 7 116551247 intron variant C/A snv 0.53 4