Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs61749409 0.882 0.080 1 94062710 missense variant G/A snv 4.4E-05 2.1E-05 4
rs61749420 0.851 0.080 1 94060740 missense variant G/A snv 1.6E-05 7.0E-06 4
rs61750120 0.882 0.160 1 94042767 missense variant G/A snv 1.2E-04 1.8E-04 4
rs61750146 0.851 0.080 1 94029522 missense variant A/G snv 8.2E-06 7.0E-06 4
rs61751389 0.925 0.040 1 94007722 frameshift variant C/- del 2.8E-05 7.0E-06 4
rs61751402 0.882 0.080 1 94029515 missense variant C/T snv 6.3E-05 5.6E-05 4
rs61751404 0.882 0.080 1 94021340 missense variant G/A;C snv 3.2E-05; 4.0E-06 4
rs61751406 0.925 0.120 1 94014622 missense variant G/T snv 2.0E-05 2.8E-05 4
rs61751407 0.882 0.080 1 94010795 splice region variant C/A;T snv 3.1E-04 3.5E-04 4
rs61753033 0.882 0.080 1 94008767 missense variant A/G snv 2.0E-05 4
rs61753038 0.851 0.080 1 94005470 stop gained G/A snv 1.2E-05 7.0E-06 4
rs886044758 0.851 0.080 1 94005511 missense variant A/G snv 4.0E-06 4
rs11806129 1 94016821 intron variant A/G;T snv 3
rs12087003 1 94037627 intron variant A/G snv 6.3E-02 3
rs1801466 1.000 1 94010911 missense variant T/A snv 4.3E-02 4.1E-02 3
rs41292677 0.882 0.080 1 94001992 missense variant C/G snv 3.0E-03 3.0E-03 3
rs481931 0.882 0.120 1 94104460 intron variant G/T snv 0.32 3
rs61748537 0.882 0.160 1 94098906 missense variant C/G;T snv 4.0E-05; 8.0E-06 3
rs61749414 0.882 0.080 1 94062611 stop gained G/A;T snv 3
rs61749423 0.925 0.040 1 94060656 stop gained G/A;T snv 8.0E-06; 4.4E-05 3
rs61749451 0.925 0.080 1 94046922 missense variant G/A;T snv 2.0E-05; 3.6E-05 3
rs61749455 0.882 0.080 1 94044692 stop gained C/A;G;T snv 5.6E-04; 4.0E-06 3
rs61750138 1.000 1 94030991 splice region variant C/A;T snv 1.2E-05 3
rs61750639 0.882 0.080 1 94007710 missense variant C/T snv 8.0E-06 1.4E-05 3
rs61750645 0.925 0.080 1 94001911 missense variant G/A;C;T snv 4.0E-06; 4.0E-06 3