Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10821515
SYK
1.000 0.080 9 90862614 intron variant G/A;C snv 1
rs13054361
TPTEP2-CSNK1E
1.000 0.080 22 38336819 intron variant G/A snv 9.3E-02 1
rs7289981
TPTEP2-CSNK1E
1.000 0.080 22 38323957 intron variant C/T snv 0.18 1
rs6772209 1.000 0.080 3 175929377 intergenic variant G/A snv 4.1E-02 2
rs8030672 1.000 0.080 15 68766745 intergenic variant T/A snv 5.4E-02 2
rs4646776
ALDH2
0.925 0.120 12 111792215 intron variant G/A;C snv 1.9E-02 5.8E-03 2
rs10058728
CSNK1A1
1.000 0.080 5 149524529 intron variant A/T snv 0.64 2
rs10842750
ITPR2
0.925 0.120 12 26537632 intron variant A/C;T snv 2
rs9868873
SEMA5B
1.000 0.080 3 123012063 intron variant G/A snv 0.28 2
rs312986 0.925 0.080 18 1898710 intron variant A/G;T snv 3
rs748676559
ACACA
0.925 0.080 17 37284932 missense variant C/T snv 4.0E-06 2.1E-05 3
rs1364898025
ATM
0.925 0.080 11 108227656 missense variant G/A snv 3
rs886063150
CA2
0.925 0.080 8 85477151 missense variant C/A;T snv 8.0E-06 3
rs7436
COL6A3
0.925 0.080 2 237324168 3 prime UTR variant T/A snv 0.10 3
rs750408412
CYP2E1
0.925 0.080 10 133538938 missense variant A/G snv 3
rs1014867
FAT4
0.925 0.080 4 125491736 missense variant C/T snv 4.9E-02 4.9E-02 3
rs1039808
FAT4
0.925 0.080 4 125318831 missense variant C/G;T snv 4.0E-06; 0.41 3
rs12508222
FAT4
0.925 0.080 4 125449492 missense variant G/A;T snv 4.3E-02; 2.0E-05 3
rs1567047
FAT4
0.925 0.080 4 125451587 missense variant G/A snv 0.27 0.22 3
rs753225272
FAT4
0.925 0.080 4 125491730 missense variant C/G;T snv 8.0E-06; 4.0E-06 3
rs770728618
IL17D
0.925 0.080 13 20721723 missense variant G/C;T snv 5.3E-05 3
rs31564
IL9
0.925 0.080 5 135894564 intron variant G/A;T snv 3
rs917870680
MDM2
0.925 0.080 12 68839304 missense variant A/G snv 3
rs2320615
NAF1
0.925 0.080 4 163148797 intron variant A/G snv 0.78 3
rs776933870
PLCE1
0.925 0.080 10 94306632 missense variant A/G snv 8.0E-06 3