Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12979860
IFNL4
0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs8099917 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 60
rs4444903
EGF
0.630 0.360 4 109912954 5 prime UTR variant A/G snv 0.51 35
rs28934571
TP53
0.645 0.360 17 7674216 missense variant C/A;G snv 31
rs6721961
NFE2L2
0.672 0.520 2 177265309 intron variant T/C;G snv 0.89 24
rs1275561861
HLA-A
0.672 0.360 6 29944350 missense variant G/A snv 23
rs12980275 0.701 0.360 19 39241143 upstream gene variant A/G snv 0.36 23
rs641738
LOC112268246 ; TMC4 ; MBOAT7
0.689 0.320 19 54173068 missense variant T/A;C;G snv 22
rs10204525
PDCD1
0.701 0.440 2 241850169 3 prime UTR variant C/T snv 0.21 20
rs2071746
HMOX1
0.708 0.320 22 35380679 intron variant A/T snv 0.49 18
rs2596542
MICA-AS1 ; MICA
0.724 0.200 6 31398818 upstream gene variant C/T snv 0.41 18
rs3077
HLA-DPA1
0.701 0.440 6 33065245 3 prime UTR variant A/G snv 0.29 16
rs1682111
ACYP2
0.742 0.240 2 54200842 intron variant A/T snv 0.56 13
rs9514828
TNFSF13B
0.752 0.440 13 108269025 intron variant C/T snv 0.35 12
rs510432
ATG5
0.752 0.280 6 106326155 upstream gene variant T/C snv 0.57 11
rs548234
ATG5
0.763 0.360 6 106120159 intron variant C/T snv 0.76 11
rs236918
PCSK7
0.776 0.160 11 117220893 non coding transcript exon variant G/A;C snv 10
rs4374383
MERTK
0.776 0.200 2 112013193 intron variant A/G snv 0.58 10
rs6834314 0.807 0.160 4 87292656 intergenic variant A/G snv 0.24 10
rs843720
ACYP2 ; LOC105374610
0.752 0.280 2 54283523 intron variant T/G snv 0.52 10
rs1041740
SOD1
0.807 0.320 21 31667849 intron variant C/T snv 0.24 8
rs4646437
CYP3A4
0.827 0.200 7 99767460 intron variant G/A snv 0.30 8
rs10053538
HAVCR2
0.807 0.160 5 157110499 intron variant C/A;T snv 7
rs11003123
MBL2
0.827 0.200 10 52771774 upstream gene variant G/A snv 0.30 6