Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10261922 1.000 0.120 7 50414314 intergenic variant C/A;G;T snv 1
rs1037351
FIGNL1 ; DDC
1.000 0.120 7 50497706 intron variant T/C snv 0.30 1
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1057519695
NRAS
0.641 0.520 1 114713907 missense variant TT/CA;CC mnv 35
rs1057519753
JAK1
0.763 0.120 1 64846664 missense variant C/A snv 9
rs1057519773
ABL1
0.851 0.160 9 130872901 missense variant T/A;C;G snv 4
rs1057519834
NRAS
0.658 0.480 1 114713908 missense variant TG/CT mnv 31
rs10740055
ARID5B
0.790 0.240 10 61958720 intron variant C/A snv 0.49 7
rs10821936
ARID5B
0.742 0.200 10 61963818 intron variant C/T snv 0.69 11
rs10821938
ARID5B
0.925 0.120 10 61965014 intron variant A/C snv 0.56 2
rs10899736
DDC ; FIGNL1
1.000 0.120 7 50479227 intron variant G/A;C snv 1
rs10949482
NHLRC1
1.000 0.120 6 18121083 3 prime UTR variant C/T snv 6.8E-02 1
rs10994982
ARID5B
0.790 0.120 10 61950345 intron variant A/G snv 0.49 7
rs11013046
PIP4K2A
1.000 0.120 10 22551654 intron variant C/T snv 0.55 1
rs1110701 1.000 0.120 7 50410929 intergenic variant A/G;T snv 1
rs11155133
LOC102723724
0.925 0.200 6 140848688 intron variant A/G snv 8.5E-02 2
rs112141546
ADAMTS18
1.000 0.120 16 77367618 missense variant C/A;G;T snv 4.0E-06; 1.4E-03 1
rs1135401746
GNB1
0.827 0.400 1 1806512 missense variant C/G snv 7
rs1142345
TPMT
0.776 0.280 6 18130687 missense variant T/C;G snv 3.7E-02 9
rs11554290
NRAS
0.583 0.600 1 114713908 missense variant T/A;C;G snv 59
rs11575387
FIGNL1 ; DDC
1.000 0.120 7 50499737 intron variant T/A;G snv 1
rs11575575
FIGNL1
1.000 0.120 7 50456510 intron variant C/A snv 7.5E-02 1
rs116855232
NUDT15
0.742 0.400 13 48045719 missense variant C/T snv 2.8E-02 1.1E-02 12
rs11770117 1.000 0.120 7 50406065 downstream gene variant A/T snv 0.41 2
rs11978267
IKZF1
0.763 0.240 7 50398606 intron variant A/G snv 0.25 9