Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs28940868
GAA
0.851 0.120 17 80112922 missense variant C/A;T snv 1.2E-04; 8.2E-06 4
rs121907936
GAA
0.882 0.120 17 80107894 missense variant T/A;C snv 4.2E-05 5.6E-05 3
rs121907942
GAA
0.882 0.120 17 80111023 missense variant C/T snv 1.6E-05 2.1E-05 3
rs1800309
GAA
0.882 0.160 17 80113242 missense variant G/A;C snv 5.6E-02; 4.4E-06 3
rs1800312
GAA
0.925 0.120 17 80117016 stop gained G/A;C snv 8.0E-06; 3.1E-04 3
rs782738646
MGAM
0.882 0.120 7 142034817 missense variant G/T snv 1.2E-05 3
rs1800307
GAA
0.925 0.120 17 80112072 missense variant G/A snv 1.8E-02 7.1E-03 2
rs374569672
GAA
0.925 0.120 17 80105866 missense variant G/A snv 7.7E-04 1.7E-04 2
rs564758226
GAA
0.925 0.120 17 80105096 synonymous variant C/T snv 5.4E-05 4.9E-05 2
rs749529161
GAA
0.925 0.120 17 80112645 stop gained C/G;T snv 4.1E-06; 1.2E-05 2
rs757700700
GAA
0.925 0.120 17 80105872 missense variant C/T snv 2.1E-05 1.4E-05 2
rs765718882
GAA
0.925 0.120 17 80118668 stop gained G/T snv 2.0E-05 7.0E-06 2
rs776948121
GAA
0.925 0.120 17 80112928 missense variant C/G;T snv 1.2E-05 2
rs1470247194
MGAM
0.925 0.120 7 142052790 missense variant A/G snv 2
rs540161721
MGAM
0.925 0.120 7 142021035 synonymous variant T/C snv 7.6E-05 3.5E-05 2
rs551975446
SI
0.925 0.120 3 165043125 missense variant G/C snv 4.8E-05 2