Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13376700 1.000 0.120 1 51011971 intergenic variant T/A snv 0.48 1
rs2292832
MIR149 ; GPC1 ; LOC100130449
0.605 0.640 2 240456086 non coding transcript exon variant T/A;C snv 0.59 46
rs763059810
CXCR4
0.623 0.600 2 136115750 missense variant T/C snv 4.0E-06 41
rs1143623
IL1B
0.677 0.440 2 112838252 upstream gene variant C/G snv 0.24 29
rs6721961
NFE2L2
0.672 0.520 2 177265309 intron variant T/C;G snv 0.89 24
rs4988235
MCM6
0.752 0.400 2 135851076 intron variant G/A;C snv 19
rs1057519921
NFE2L2
0.763 0.240 2 177234231 missense variant T/C snv 10
rs6713088
ACYP2
0.763 0.200 2 54118332 intron variant C/G snv 0.48 9
rs3783521
IL1A
0.807 0.200 2 112786000 upstream gene variant G/A snv 0.26 8
rs1057519920
NFE2L2
0.790 0.160 2 177234232 missense variant C/A;G;T snv 7
rs843711
ACYP2
0.790 0.200 2 54251980 intron variant C/T snv 0.41 7
rs3783546
IL1A
0.882 0.160 2 112777253 intron variant G/C snv 0.70 5
rs3783550
IL1A
0.827 0.200 2 112775308 intron variant G/T snv 0.64 0.70 5
rs11894252
EPAS1
0.925 0.120 2 46306237 intron variant T/A;C;G snv 3
rs1609682
IL1A
0.882 0.160 2 112782628 intron variant G/T snv 0.70 3
rs553863637
PLEK
0.925 0.120 2 68382602 missense variant G/A;C snv 4.8E-05 3
rs11689011
EPAS1
1.000 0.120 2 46314037 intron variant T/A;C;G snv 2
rs12617313
EPAS1
0.925 0.120 2 46332637 intron variant A/G;T snv 2
rs755415626
SF3B1
0.925 0.200 2 197401887 missense variant C/T snv 7.0E-06 2
rs7579899
EPAS1
0.925 0.120 2 46310465 intron variant A/G snv 0.52 2
rs9679290
EPAS1
0.925 0.120 2 46330505 intron variant G/C snv 0.41 2
rs10211665
EPAS1
1.000 0.120 2 46298957 intron variant T/C snv 0.58 1
rs11125068
EPAS1
1.000 0.120 2 46300677 intron variant A/G snv 0.62 1
rs11684885
EPAS1
1.000 0.120 2 46306413 intron variant T/C;G snv 1
rs12105521
ZEB2
1.000 0.120 2 144450769 intron variant G/A;T snv 1