Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2228467
CYP8B1 ; KRBOX1 ; ACKR2
1.000 0.080 3 42864624 missense variant T/C snv 5.1E-02 4.7E-02 8
rs4760
PLAUR
1.000 0.080 19 43648948 missense variant A/G snv 0.12 0.11 8
rs56378716
MPO
1.000 0.080 17 58279141 missense variant A/G snv 1.0E-02 9.8E-03 6
rs10795656 1.000 0.080 10 8553876 intergenic variant G/A;T snv 4
rs113473633
NFKB1
1.000 0.040 4 102527974 intron variant A/G snv 1.6E-02 4
rs2033784
SMAD3
1.000 0.080 15 67157322 intron variant A/G snv 0.35 4
rs2381416 1.000 0.080 9 6193455 upstream gene variant C/A snv 0.65 4
rs1036207
NDFIP1
1.000 0.080 5 142119476 intron variant A/G;T snv 3
rs114269697
JAK1
1.000 0.040 1 64848529 intron variant C/A snv 7.3E-03 3
rs12935413
CLEC16A
1.000 0.080 16 11116590 intron variant G/A snv 0.34 3
rs2248116
IRF1-AS1
1.000 0.040 5 132468655 intron variant C/A snv 0.70 3
rs3893464
HLA-A
1.000 0.120 6 29967473 downstream gene variant G/A snv 0.46 3
rs4807542
GPX4
1.000 0.120 19 1104079 synonymous variant G/A;C snv 0.22; 1.8E-05 3
rs61840192 1.000 0.080 10 9001441 intergenic variant G/A;C;T snv 3
rs8046011 1.000 0.120 16 11226805 downstream gene variant G/A;T snv 3
rs9504361
EXOC2
1.000 0.040 6 577820 intron variant A/G snv 0.40 3
rs10086568 1.000 0.120 8 7042814 upstream gene variant G/A snv 0.34 2
rs149467613
P2RY2
1.000 0.040 11 73232438 intron variant G/A snv 3.3E-02 2
rs3181077
CCR1 ; CCR3
1.000 0.080 3 46209161 intron variant C/T snv 0.80 2
rs8015478
CEBPE
1.000 0.120 14 23116809 downstream gene variant A/C snv 0.68 2
rs9314614
GS1-24F4.2
1.000 0.120 8 6840209 intron variant C/G snv 0.61 2
rs385893 0.925 0.080 9 4763176 downstream gene variant T/C snv 0.44 9
rs6740847 0.925 0.040 2 181443625 intergenic variant A/G snv 0.57 8
rs12440045 0.925 0.080 15 41490486 upstream gene variant A/C snv 0.67 6
rs2239630
CEBPE
0.925 0.160 14 23120140 upstream gene variant A/C;G snv 6