Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3112831 1.000 0.080 1 94078678 missense variant T/C;G snv 0.26 0.26 2
rs1801466 1.000 1 94010911 missense variant T/A snv 4.3E-02 4.1E-02 3
rs1801581 0.925 0.080 1 94047009 missense variant C/A;T snv 2.8E-05; 3.0E-02 2
rs1800555 1.000 0.040 1 93998061 missense variant C/T snv 1.1E-02 1.0E-02 1
rs61750126 0.925 0.080 1 94040048 missense variant A/C snv 6.7E-03 2.8E-02 2
rs61750129 1.000 1 94032007 missense variant C/T snv 5.1E-03 2.0E-02 1
rs1800553 0.742 0.240 1 94008251 missense variant C/T snv 4.7E-03 3.0E-03 17
rs1800549 0.925 0.040 1 94030497 missense variant G/A snv 4.6E-03 1.6E-03 2
rs76157638 0.851 0.080 1 94051698 missense variant C/G;T snv 4.4E-03; 4.0E-06 6
rs28938473 0.882 0.040 1 94007731 missense variant G/A snv 3.0E-03 3.6E-03 4
rs41292677 0.882 0.080 1 94001992 missense variant C/G snv 3.0E-03 3.0E-03 3
rs145525174 1.000 1 94063218 missense variant C/T snv 2.7E-03 2.4E-03 1
rs62646862 1.000 1 94103130 missense variant C/A;T snv 1.6E-05; 2.6E-03 1
rs17110922 1 94043489 intron variant A/T snv 2.5E-03 9.9E-03 2
rs113106943 0.925 0.040 1 94021848 missense variant C/T snv 2.4E-03 2.3E-03 2
rs61751374 0.776 0.160 1 94043413 missense variant G/A snv 1.7E-03 1.7E-03 10
rs56357060 1.000 1 94030483 missense variant C/T snv 1.6E-03 1.8E-03 1
rs1800552 0.851 0.080 1 94010821 missense variant C/T snv 1.6E-03 1.5E-03 4
rs61754024 1.000 1 94062586 missense variant A/C snv 1.5E-03 1.7E-03 1
rs62642564 0.925 0.040 1 94001068 missense variant C/G;T snv 1.5E-03 2
rs62646863 1.000 1 94103119 missense variant T/C snv 1.5E-03 2.2E-03 1
rs61749417 1.000 1 94062587 missense variant C/T snv 1.3E-03 4.8E-03 1
rs61749440 1.000 1 94048921 missense variant G/A snv 1.2E-03 1.3E-03 1
rs1762111 0.851 0.080 1 94021934 missense variant A/G snv 1.2E-03 1.3E-03 5
rs61749435 1.000 1 94055152 missense variant A/G snv 1.1E-03 3.8E-03 1