Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs77375493
INSL6 ; JAK2
0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 187
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs121434592
AKT1
0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 34
rs4925
GSTO1
0.677 0.560 10 104263031 missense variant C/A snv 0.25 0.23 28
rs121913459
ABL1
0.672 0.160 9 130872896 missense variant C/T snv 25
rs156697
GSTO2
0.672 0.560 10 104279427 missense variant A/G;T snv 0.35 25
rs1057519743
CRLF2
0.827 0.120 Y 1196852 missense variant A/C snv 6
rs866838052
GSTK1 ; LOC105375545
0.851 0.160 7 143267618 missense variant C/A snv 6
rs62527607
BAALC ; BAALC-AS2
0.827 0.160 8 103141321 non coding transcript exon variant G/T snv 0.14 5
rs780634396
BCL2
0.882 0.120 18 63318618 missense variant T/C snv 4.0E-06 5
rs1057519721
INSL6 ; JAK2
0.882 0.120 9 5078360 missense variant A/G snv 4
rs4958351
GRIA1
0.882 0.120 5 153790814 intron variant G/A;T snv 0.31 3
rs11980379
IKZF1
0.882 0.120 7 50402283 3 prime UTR variant T/C snv 0.25 3
rs189434316 0.925 0.120 14 92231568 intergenic variant A/T snv 4.1E-02 2
rs2393732
ARID5B
0.925 0.120 10 62007470 intron variant G/A snv 0.15 2
rs4948488
ARID5B
0.925 0.120 10 61925395 intron variant C/A;T snv 2
rs1057519723
JAK2 ; INSL6
0.925 0.120 9 5078362 missense variant A/C;G;T snv 2
rs529311209
SGSM3
0.925 0.120 22 40409754 missense variant G/A;C;T snv 3.3E-05; 8.2E-06 2
rs12430881
FLT3
1.000 0.120 13 28020665 intron variant T/C snv 0.28 1
rs35958982
FLT3
1.000 0.120 13 28034336 missense variant C/T snv 1.3E-02 5.0E-02 1
rs1346944271
JAK2 ; INSL6
1.000 0.120 9 5090497 missense variant G/A snv 1.4E-05 1
rs3780135
PAX5
1.000 0.120 9 36840626 missense variant G/A snv 0.88 0.77 1