Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519758
ABL1
1.000 0.080 9 130872153 missense variant T/G snv 1
rs1057519771
ABL1
1.000 0.080 9 130872201 missense variant G/C snv 2
rs1057519772
ABL1
1.000 0.080 9 130872895 missense variant A/G snv 1
rs121913459
ABL1
0.672 0.160 9 130872896 missense variant C/T snv 25
rs1057519773
ABL1
0.851 0.160 9 130872901 missense variant T/A;C;G snv 4
rs1057519774
ABL1
1.000 0.080 9 130872902 missense variant T/G snv 1
rs121913451
ABL1
0.851 0.160 9 130872903 missense variant C/A;G snv 4
rs121913457
ABL1
1.000 0.080 9 130873004 missense variant T/C snv 1
rs121913450
ABL1
1.000 0.080 9 130873016 missense variant A/G snv 1
rs121913452
ABL1
0.851 0.080 9 130873027 missense variant T/A;C;G snv 4
rs1057519775
ABL1
1.000 0.080 9 130873028 missense variant T/G snv 1
rs121913454
ABL1
0.925 0.080 9 130874969 missense variant A/G snv 2
rs1064156
ABL1
1.000 0.080 9 130878519 missense variant G/A snv 4.0E-06 1
rs886063722
AGPAT2
1.000 0.080 9 136677118 missense variant G/A snv 4.0E-06 1
rs121913370
BRAF
0.763 0.360 7 140753393 missense variant T/C;G snv 10
rs6931104
ARMT1
1.000 0.080 6 151465042 intron variant G/A snv 0.54 1
rs683369
SLC22A1
0.807 0.360 6 160130172 missense variant G/A;C;T snv 4.0E-06; 0.83; 4.0E-06 7
rs628031
SLC22A1
0.807 0.280 6 160139813 missense variant A/C;G snv 5.3E-05; 0.63 8
rs45511401
ABCC1
0.851 0.120 16 16079375 missense variant G/T snv 3.8E-02 3.6E-02 4
rs4148356
ABCC1
0.851 0.120 16 16083418 missense variant G/A snv 2.3E-02 1.3E-02 4
rs532354124
ASPM
1.000 0.080 1 197103274 missense variant T/C;G snv 1
rs4149117
SLCO1B3-SLCO1B7 ; SLCO1B3
0.763 0.360 12 20858546 missense variant T/C;G snv 0.81 15
rs375912312
EPHA8
1.000 0.080 1 22588916 missense variant C/T snv 7.0E-06 1
rs369488601
RSPH14 ; BCR
1.000 0.080 22 23181175 missense variant G/A;C snv 1.9E-05; 9.7E-05 1
rs775014154
RSPH14 ; BCR
1.000 0.080 22 23181637 missense variant C/T snv 5.8E-05 7.0E-05 1