Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs8099917 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 60
rs12980275 0.701 0.360 19 39241143 upstream gene variant A/G snv 0.36 23
rs6834314 0.807 0.160 4 87292656 intergenic variant A/G snv 0.24 10
rs3135363 0.776 0.360 6 32421871 intergenic variant A/G snv 0.24 8
rs41295061 0.790 0.360 10 6072697 upstream gene variant C/A snv 6.1E-02 8
rs11977021 0.827 0.240 7 106288069 upstream gene variant C/T snv 0.22 5
rs3129859 0.827 0.320 6 32433162 intergenic variant G/C;T snv 5
rs3844942 0.882 0.120 4 189571800 intergenic variant T/C snv 3
rs343064 0.925 0.080 7 35515178 upstream gene variant C/G;T snv 2
rs643608 0.925 0.080 21 43348682 intergenic variant C/T snv 0.69 2
rs6487679 0.925 0.080 12 9218736 intergenic variant C/T snv 0.80 2
rs8021276 0.925 0.080 14 92110162 upstream gene variant A/G;T snv 2
rs9380516 0.925 0.120 6 35534425 TF binding site variant T/C snv 0.85 2
rs2287622
ABCB11
0.724 0.240 2 168973818 missense variant A/C;G;T snv 0.57 16
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs1682111
ACYP2
0.742 0.240 2 54200842 intron variant A/T snv 0.56 13
rs843645
ACYP2
0.827 0.120 2 54247527 intron variant T/A;G snv 0.19 5
rs843720
ACYP2 ; LOC105374610
0.752 0.280 2 54283523 intron variant T/G snv 0.52 10
rs10020432
AFP
0.925 0.080 4 73455883 3 prime UTR variant A/G snv 0.54 2
rs2298839
AFP
0.925 0.080 4 73445127 splice region variant A/G;T snv 0.54 2
rs6834059
AFP
0.925 0.080 4 73435958 intron variant C/G snv 0.23 2
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs4762
AGT
0.637 0.440 1 230710231 missense variant G/A snv 0.12 0.11 35
rs56073403
AGT
0.882 0.160 1 230710009 missense variant T/C snv 7.2E-04 6.8E-04 3
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116