Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs545854 0.882 0.160 8 10002570 intron variant G/C snv 0.85 4
rs2453626
RGS22
1.000 0.080 8 100125669 intron variant T/A;C snv 1
rs1799768
SERPINE1
0.807 0.360 7 101126425 upstream gene variant -/A;C ins 6
rs532966772
SERPINE1
1.000 0.080 7 101132023 synonymous variant C/T snv 4.0E-06 1
rs2038366
S1PR1 ; LOC101928370
1.000 0.080 1 101235342 upstream gene variant G/T snv 0.32 1
rs59317557
S1PR1 ; LOC101928370
1.000 0.080 1 101236367 non coding transcript exon variant C/G snv 0.37 1
rs3753194
S1PR1 ; LOC101928370
1.000 0.080 1 101237269 intron variant A/G snv 6.8E-02 1
rs28665122
SELENOS
0.807 0.240 15 101277522 upstream gene variant C/T snv 0.24 7
rs13022699 1.000 0.080 2 101671373 intergenic variant C/T snv 5.3E-02 1
rs12468899
MAP4K4
1.000 0.080 2 101809678 intron variant A/G;T snv 1
rs1709393
LINC02085
1.000 0.080 3 101980310 intron variant C/T snv 0.55 2
rs13427957
IL1R1
1.000 0.080 2 102072571 intron variant C/T snv 0.46 1
rs11225138
YAP1
0.925 0.200 11 102123167 intron variant G/C snv 6.1E-02 2
rs949963
IL1R1
0.925 0.160 2 102153326 intron variant C/T snv 0.22 3
rs871657
IL1R1
1.000 0.080 2 102154881 intron variant C/T snv 0.22 2
rs74180212 0.925 0.080 2 102181785 intron variant T/C;G snv 2
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49
rs10189629 1.000 0.080 2 102263004 regulatory region variant C/A snv 0.15 2
rs78545931 0.925 0.080 2 102265892 intergenic variant A/G snv 0.16 2
rs11692065 1.000 0.080 2 102267515 intergenic variant C/T snv 0.15 2
rs11674302 1.000 0.080 2 102270668 intergenic variant T/C snv 0.16 2
rs60227565 0.925 0.080 2 102275879 intergenic variant G/A;T snv 0.10 2
rs202011557 1.000 0.080 2 102297182 intergenic variant -/CAA delins 1
rs10515922 1.000 0.080 2 102298194 regulatory region variant A/G snv 6.9E-02 1
rs12470864
IL1RL1
0.925 0.080 2 102309902 upstream gene variant G/A snv 0.30 4