Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs529311209
SGSM3
0.925 0.120 22 40409754 missense variant G/A;C;T snv 3.3E-05; 8.2E-06 2
rs1057519752
MPL
1.000 0.080 1 43349307 missense variant A/C;G;T snv 1
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
rs1259653415
TFRC
1.000 0.080 3 196071416 missense variant T/C snv 7.0E-06 3
rs556915505
MECOM
0.851 0.080 3 169143780 missense variant T/C snv 4.0E-06 7.0E-06 5
rs778767225
MOK
0.851 0.200 14 102231805 missense variant C/A snv 2.4E-05 7.0E-06 4
rs1200469268
ABCA1
0.925 0.080 9 104830968 missense variant C/A snv 7.0E-06 2
rs764634461
JAK2 ; INSL6
1.000 0.080 9 5072516 missense variant T/G snv 1.2E-05 2.8E-05 1
rs201478192
KIDINS220
0.790 0.200 2 8731667 missense variant C/A snv 2.4E-04 2.6E-04 12
rs17292650
MPL
0.882 0.120 1 43338136 missense variant G/T snv 3.5E-03 1.4E-02 3
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs16754
WT1
0.732 0.240 11 32396399 synonymous variant T/C snv 0.24; 4.0E-06 0.17 15
rs12342421
JAK2 ; INSL6
0.851 0.080 9 5065750 intron variant G/C snv 0.23 5
rs4495487
INSL6 ; JAK2
0.925 0.080 9 5072798 intron variant T/C snv 0.23 3
rs9376092
LOC105378010
0.851 0.120 6 135106006 upstream gene variant C/A snv 0.24 10
rs10974944
JAK2 ; INSL6
0.882 0.160 9 5070831 intron variant C/G snv 0.25 4
rs12343867
INSL6 ; JAK2
0.790 0.200 9 5074189 intron variant T/C snv 0.25 9
rs59384377
INSL6 ; JAK2
1.000 0.080 9 5005034 intron variant A/T snv 0.26 1
rs12339666
INSL6 ; JAK2
0.925 0.080 9 5063296 intron variant G/T snv 0.34 3
rs2736100
TERT
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs2201862 0.925 0.080 3 168930251 downstream gene variant T/C snv 0.63 3