Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4845618
IL6R
0.851 0.160 1 154427539 intron variant G/T snv 0.53 5
rs12083537
IL6R
0.882 0.200 1 154408627 intron variant A/G snv 0.22 4
rs4845623
IL6R
0.925 0.040 1 154443301 intron variant A/G snv 0.47 4
rs61812598
IL6R
1.000 0.080 1 154447611 intron variant G/A snv 0.31 4
rs7518199
IL6R
1 154434943 intron variant A/C;T snv 0.39; 4.2E-06 4
rs12034383
CR1
1 207630250 intron variant G/A snv 0.47 3
rs12133641
IL6R
0.925 0.040 1 154455807 intron variant A/G snv 0.44 3
rs12741825 1 159700355 downstream gene variant C/T snv 0.24 3
rs12753193 1 65703996 non coding transcript exon variant G/A snv 0.58 3
rs2808629 0.925 0.160 1 159707006 upstream gene variant G/A snv 0.31 3
rs3027012
CADM3-AS1 ; ACKR1
1 159204333 5 prime UTR variant C/T snv 0.13 3
rs3093068 1.000 0.040 1 159711574 downstream gene variant G/C snv 0.13 3
rs4660808
PPIEL
1 39552837 intron variant C/T snv 0.17 3
rs661955 1 234707109 upstream gene variant G/C;T snv 3
rs7549785
FCER1A
0.925 0.080 1 159308078 3 prime UTR variant G/A snv 0.13 3
rs876537
CRPP1
1.000 0.080 1 159705143 non coding transcript exon variant C/T snv 0.34 3
rs10908713 1 159369769 intron variant T/C snv 0.47 2
rs11208722 1 65705318 intron variant C/A snv 0.75 2
rs11265174 1 159350569 intron variant T/A snv 0.35 2
rs11265190
OR10J1
1 159421611 intron variant G/A snv 0.47 2
rs11265191
OR10J1 ; OR10J4
1 159430569 intron variant C/G;T snv 2
rs11265196 1 159448422 intron variant G/A snv 0.47 2
rs11265260 1.000 0.080 1 159730249 intergenic variant A/G snv 6.8E-02 2
rs11265263 1 159740727 intergenic variant C/A;T snv 2
rs1127311
ADAR ; CHRNB2
1 154584187 3 prime UTR variant G/A snv 0.42 2