Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10983755 0.790 0.320 9 117702392 upstream gene variant G/A snv 3.2E-02 7
rs1917799 0.851 0.120 10 49542929 upstream gene variant A/C snv 0.25 4
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv 34
rs1130233
AKT1
0.742 0.480 14 104773557 synonymous variant C/T snv 0.30 0.23 13
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs7804372
CAV1
0.716 0.320 7 116554174 intron variant T/A snv 0.27 19
rs3807987
CAV1
0.732 0.280 7 116539780 intron variant G/A snv 7.6E-02 17
rs2243086
CHRNE ; GP1BA
1.000 0.040 17 4930914 intron variant G/T snv 0.20 2
rs6490061
CUX2
0.925 0.120 12 111335541 intron variant T/C snv 0.30 2
rs2376549
DEFB121
0.925 0.120 20 31411284 intron variant C/T snv 0.42 2
rs10420321
DNMT1
0.925 0.080 19 10189741 intron variant A/G snv 0.11 2
rs8111085
DNMT1
1.000 0.040 19 10162696 missense variant T/A;C;G snv 1
rs1550117
DNMT3A
0.790 0.320 2 25343038 upstream gene variant A/G;T snv 11
rs158572
ERCC8 ; NDUFAF2
0.851 0.120 5 60943616 intron variant G/A snv 0.63 4
rs601338
FUT2 ; LOC105447645
0.742 0.280 19 48703417 stop gained G/A snv 0.38 0.45 19
rs3805246
GAB1
0.882 0.120 4 143382955 intron variant G/A snv 0.31 3
rs3024496
IL10
0.827 0.200 1 206768519 3 prime UTR variant A/G snv 0.43 6
rs2275913
IL17A
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs3748067
IL17A
0.672 0.320 6 52190541 3 prime UTR variant C/T snv 6.2E-02 21
rs763780
IL17F
0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 87
rs1800896
IL19 ; IL10
0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1878672
IL19 ; IL10
0.882 0.080 1 206770368 intron variant G/A;C;T snv 3
rs3024491
IL19 ; IL10
0.925 0.040 1 206771701 intron variant C/A;T snv 2
rs1143627
IL1B
0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56 47