Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs67376798
DPYD
0.851 0.120 1 97082391 missense variant T/A snv 2.8E-03 3.3E-03 9
rs104894419
LIG4
0.807 0.360 13 108208829 stop gained G/A snv 9.9E-05 7.0E-05 8
rs1554785242
ADAMTS13
0.882 0.160 9 133426240 missense variant G/T snv 8
rs1554791280
ADAMTS13
0.882 0.160 9 133442718 missense variant T/C snv 8
rs483352867
STIM1
0.827 0.400 11 4074620 missense variant C/T snv 8
rs104894816
GATA1
0.827 0.120 X 48792377 missense variant A/G snv 6
rs2297630
CXCL12
0.827 0.160 10 44376100 intron variant G/A;T snv 0.21 6
rs724159947
ETV6
0.851 0.120 12 11869601 missense variant C/T snv 6
rs757788894
CLCN7
0.882 0.120 16 1449081 missense variant C/T snv 4.0E-06 6
rs121908065
CHRNE ; GP1BA
0.851 0.080 17 4933119 missense variant C/T snv 5
rs146249964
MPL
0.851 0.080 1 43337929 splice donor variant T/A snv 4.0E-04 1.7E-04 5
rs1553196096
CDC42
1 22086463 missense variant G/A snv 5
rs5030764
GP9
0.882 0.080 3 129061921 missense variant A/G snv 4.8E-04 7.4E-04 5
rs61749384
VWF
0.882 0.080 12 6019502 missense variant G/A snv 5
rs735239
CD209
0.851 0.240 19 7748382 upstream gene variant A/G snv 0.26 5
rs74315450
RUNX1
0.851 0.120 21 34859485 missense variant C/T snv 5
rs878853314
GBA
0.882 0.240 1 155239655 missense variant C/G snv 5
rs878853315
GBA
0.925 0.160 1 155236292 missense variant G/C snv 5
rs121909752
SEPT5-GP1BB ; GP1BB ; SEPTIN5
0.925 0.080 22 19723980 stop gained G/A;C snv 7.5E-06 4
rs143873938
FLNA
0.882 0.120 X 154365245 missense variant C/A;G;T snv 3.1E-03 4
rs1537514
C1orf167 ; MTHFR
0.882 0.120 1 11788011 missense variant G/C snv 0.10 0.10 4
rs1554162524
ELOVL4
0.882 0.160 6 79925034 splice acceptor variant T/C snv 4
rs2274407
ABCC4
0.882 0.120 13 95206781 missense variant C/A;G;T snv 9.7E-02 0.10 4
rs28928907
MPL
0.882 0.160 1 43338634 missense variant G/A;C snv 8.0E-06; 3.8E-04 4
rs3814055
NR1I2
0.925 0.040 3 119781188 5 prime UTR variant C/T snv 0.35 4