Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs72552778 0.827 0.040 7 87447080 missense variant G/A snv 1.6E-04 1.7E-04 5
rs1382897404 0.851 0.040 2 169018071 missense variant C/G snv 7.0E-06 4
rs1257887155 0.925 0.040 7 87440228 missense variant C/T snv 7.0E-06 2
rs387906528 0.925 0.040 7 87443346 frameshift variant CT/TTG delins 2
rs765478923 0.925 0.040 7 87447182 missense variant G/A snv 1.6E-05 2.8E-05 2
rs8187788 0.925 0.040 7 87462827 missense variant G/C snv 7.2E-04 7.3E-04 2
rs121918442 1.000 0.040 7 87406293 missense variant G/A;T snv 2.4E-05 1
rs1262922848 1.000 0.040 7 87408066 missense variant G/A snv 1
rs1408217402 1.000 0.040 7 87454583 missense variant G/A snv 4.0E-06 1
rs1411970557 1.000 0.040 7 87462811 missense variant A/C snv 4.0E-06 7.0E-06 1
rs141677867 1.000 0.040 7 87423940 missense variant G/A snv 8.0E-06 7.0E-06 1
rs142794414 1.000 0.040 7 87472655 missense variant G/A;T snv 4.8E-04; 8.0E-06; 4.0E-06 1.2E-03 1
rs372685632 1.000 0.040 7 87462904 missense variant C/T snv 8.8E-05 6.3E-05 1
rs397514620 1.000 0.040 7 87439765 missense variant G/A;C snv 8.0E-06 1
rs571555115 1.000 0.040 7 87431519 missense variant G/A snv 3.2E-05 2.8E-05 1
rs72552776 1.000 0.040 7 87431525 missense variant A/T snv 4.0E-06 1
rs72552779 1.000 0.040 7 87447137 missense variant A/G snv 1
rs759787957 1.000 0.040 7 87411894 missense variant G/C snv 4.0E-06 1
rs761238221 1.000 0.040 7 87439752 missense variant C/A;T snv 8.0E-06; 3.6E-05 1
rs780641693 1.000 0.040 7 87462832 missense variant A/T snv 4.0E-06 1
rs8187797 1.000 0.040 7 87439814 missense variant C/G snv 2.1E-03 8.7E-03 1
rs970324585 1.000 0.040 7 87423931 missense variant G/A snv 1
rs972726699 1.000 0.040 7 87426875 missense variant C/T snv 8.0E-06 7.0E-06 1
rs1051861187 0.827 0.080 7 87409385 missense variant A/G snv 6
rs375315619 0.851 0.080 7 87440230 missense variant T/C snv 2.0E-04 9.8E-05 4