Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12339666
INSL6 ; JAK2
0.925 0.080 9 5063296 intron variant G/T snv 0.34 3
rs4495487
INSL6 ; JAK2
0.925 0.080 9 5072798 intron variant T/C snv 0.23 3
rs1200469268
ABCA1
0.925 0.080 9 104830968 missense variant C/A snv 7.0E-06 2
rs12340895
INSL6 ; JAK2
1.000 0.080 9 5076691 intron variant C/A;G snv 1
rs1441084781
TLR4
1.000 0.080 9 117712543 missense variant G/A;T snv 4.0E-06 1
rs59384377
INSL6 ; JAK2
1.000 0.080 9 5005034 intron variant A/T snv 0.26 1
rs764634461
JAK2 ; INSL6
1.000 0.080 9 5072516 missense variant T/G snv 1.2E-05 2.8E-05 1
rs562015640
PTEN
0.742 0.360 10 87960957 stop gained A/G;T snv 1.2E-05 16
rs104894230
HRAS ; LRRC56
0.564 0.600 11 534288 missense variant C/A;G;T snv 73
rs727503094
LRRC56 ; HRAS
0.633 0.440 11 534287 missense variant GC/AG;AT;TA;TT mnv 41
rs16754
WT1
0.732 0.240 11 32396399 synonymous variant T/C snv 0.24; 4.0E-06 0.17 15
rs121913529
KRAS
0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144
rs121918464
PTPN11
0.708 0.440 12 112450406 missense variant G/A;C snv 25
rs121918462
PTPN11
0.742 0.320 12 112450398 missense variant C/T snv 13
rs104894365
KRAS
0.827 0.320 12 25245345 missense variant C/T snv 9
rs397507510
PTPN11
0.776 0.280 12 112450361 missense variant G/A;C;T snv 8
rs778767225
MOK
0.851 0.200 14 102231805 missense variant C/A snv 2.4E-05 7.0E-06 4
rs121913502
IDH2
0.708 0.320 15 90088702 missense variant C/A;T snv 3.2E-05 19
rs1057519819
MAP2K1
0.851 0.240 15 66436750 missense variant T/C snv 6
rs17849241
SOCS3 ; LOC101928674
0.925 0.080 17 78358688 missense variant G/C;T snv 4.1E-06; 2.1E-04 3
rs121913504
JAK3
0.882 0.080 19 17837200 missense variant G/A snv 3
rs529311209
SGSM3
0.925 0.120 22 40409754 missense variant G/A;C;T snv 3.3E-05; 8.2E-06 2