Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 41
rs780093
GCKR
0.763 0.240 2 27519736 intron variant T/C snv 0.68 30
rs2227306
CXCL8
0.677 0.680 4 73741338 intron variant C/T snv 0.31 21
rs2149356
TLR4
0.742 0.360 9 117711921 intron variant T/G snv 0.54 14
rs10774625
ATXN2
0.763 0.320 12 111472415 intron variant A/G snv 0.66 13
rs2068834
ZNF512
0.925 0.120 2 27616672 intron variant T/C snv 0.28 10
rs780092
GCKR
0.827 0.160 2 27520287 intron variant A/G snv 0.18 10
rs11613352
R3HDM2
0.827 0.160 12 57398797 intron variant C/T snv 0.19 9
rs17145750
MLXIPL
0.925 0.120 7 73612048 intron variant C/A;T snv 9
rs2244608
HNF1A ; HNF1A-AS1
0.882 0.160 12 120979185 intron variant A/G snv 0.29 9
rs9472135
LOC107986598
0.925 0.120 6 43842065 intron variant T/A;C;G snv 9
rs4766578
ATXN2
0.851 0.200 12 111466567 intron variant T/A snv 0.66 8
rs1106766
R3HDM2
0.882 0.120 12 57415673 intron variant C/T snv 0.19 7
rs11755724
RREB1
0.807 0.320 6 7118757 intron variant A/G;T snv 7
rs13022873
ZNF512
0.882 0.120 2 27592643 intron variant A/C;T snv 7
rs1394125
UBE2Q2
0.882 0.200 15 75866642 intron variant G/A;T snv 7
rs1572982
HFE
0.827 0.200 6 26094139 intron variant G/A;T snv 0.52; 8.0E-06 7
rs3817588
GCKR
0.882 0.160 2 27508345 intron variant T/C snv 0.14 7
rs6449213
SLC2A9 ; LOC105374476
0.827 0.240 4 9992591 intron variant C/T snv 0.82 7
rs6855911
SLC2A9
0.851 0.200 4 9934286 intron variant A/G snv 0.33 7
rs734553
SLC2A9
0.851 0.240 4 9921380 intron variant G/A;T snv 7
rs737267
SLC2A9
0.851 0.240 4 9933120 intron variant G/A;T snv 7
rs7691759 0.882 0.120 4 9686390 intron variant T/A;C snv 7
rs7811265
BAZ1B
0.925 0.120 7 73520180 intron variant A/G snv 0.23 7