Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs223469
LOC102723704
1.000 0.040 4 102778621 intergenic variant T/C snv 0.99 1
rs908832
ABCA2
0.851 0.120 9 137018032 missense variant A/C;G snv 0.97 0.96 4
rs222826 0.851 0.120 2 146120964 regulatory region variant T/C snv 0.94 16
rs7190256
ZFHX3
0.851 0.120 16 72963084 intron variant C/T snv 0.94 16
rs6932003
LINC00240
1.000 0.040 6 27022412 intron variant T/C snv 0.94 1
rs9326246 0.925 0.040 11 116741017 intergenic variant C/G snv 0.93 9
rs9261588
HCG17
1.000 0.040 6 30243030 intron variant T/G snv 0.92 1
rs3130933
POU5F1 ; TCF19
0.882 0.200 6 31164308 intron variant T/C snv 0.92 3
rs3094065
HCG17 ; HCG18
1.000 0.040 6 30314555 intron variant T/C snv 0.92 1
rs4576240
KIAA0319
1.000 0.040 6 24596250 missense variant T/A;G snv 4.0E-06; 0.92 0.91 1
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 33
rs505151
PCSK9
0.732 0.360 1 55063514 missense variant G/A snv 0.95 0.90 18
rs7250581 1.000 0.040 19 29573489 intergenic variant A/G snv 0.89 1
rs911178
ZBED9
0.925 0.120 6 28606638 intron variant T/C snv 0.89 2
rs6601299
LOC157273
0.925 0.040 8 9327181 intron variant T/C snv 0.88 5
rs471364
TTC39B
1.000 0.040 9 15289580 intron variant C/T snv 0.87 3
rs2230301
EPRS1
1.000 0.040 1 220024283 missense variant G/T snv 0.84 0.86 1
rs864265 0.925 0.080 3 186836503 intergenic variant T/G snv 0.86 4
rs891512
NOS3
0.925 0.040 7 151011001 intron variant A/G snv 0.84 0.85 4
rs2288904
SLC44A2
0.807 0.240 19 10631494 missense variant A/G snv 0.80 0.83 8
rs562556
PCSK9
0.827 0.280 1 55058564 missense variant G/A snv 0.86 0.83 8
rs10767664
BDNF
0.752 0.400 11 27704439 intron variant T/A snv 0.83 16
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs133049
MRTFA
0.882 0.080 22 40635351 intron variant A/- delins 0.82 4
rs2158041
AHR
0.807 0.160 7 17328796 intron variant T/C snv 0.81 6