Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs532728316 0.882 0.080 20 3230205 missense variant C/T snv 1.0E-04 3.5E-05 3
rs767468885 0.925 0.080 6 38761702 missense variant G/A snv 5.5E-06 7.0E-06 2
rs121909387 0.925 0.080 20 3228684 missense variant C/T snv 4.0E-06 2
rs121909388 0.925 0.080 20 3230258 missense variant G/A snv 1.2E-05 7.0E-06 2
rs121909389 0.925 0.080 20 3230587 missense variant C/T snv 4.0E-06 2
rs121909391 0.925 0.080 20 3228260 missense variant G/A snv 8.0E-06 2
rs121909392 0.925 0.080 20 3228259 missense variant C/T snv 1.2E-05 2
rs1191074716 1.000 0.080 20 3231514 missense variant G/A snv 4.0E-06 1
rs1276051624 1.000 0.080 20 3234280 missense variant C/T snv 4.0E-06 1
rs1298347142 1.000 0.080 20 3231520 missense variant G/A snv 7.0E-06 1
rs1422526172 1.000 0.080 20 3228367 missense variant G/A snv 7.0E-06 1
rs1465111896 1.000 0.080 20 3228630 missense variant G/A snv 1
rs1482631297 1.000 0.080 20 3234227 stop gained C/A;G;T snv 4.0E-06; 8.0E-06; 4.0E-06 1
rs200106947 1.000 0.080 20 3234786 missense variant C/A;T snv 1.2E-04; 1.2E-05 1
rs566507872 1.000 0.080 20 3233949 missense variant G/A;T snv 1.2E-05; 1.2E-05 1
rs749826950 1.000 0.080 20 3229137 missense variant T/C;G snv 2.4E-05 1
rs752287261 1.000 0.080 20 3234176 missense variant C/T snv 4.8E-05 4.9E-05 1
rs757244518 1.000 0.080 20 3228395 missense variant C/T snv 1.2E-05 7.0E-06 1
rs757553189 1.000 0.080 20 3228685 missense variant G/A;T snv 8.0E-06 1
rs759667344 1.000 0.080 20 3233936 missense variant G/A snv 8.0E-06 1
rs762942751 1.000 0.080 20 3233594 missense variant G/A snv 1.2E-05 1.4E-05 1
rs766567944 1.000 0.080 20 3228537 missense variant C/T snv 1.2E-05 7.0E-06 1
rs780171125 1.000 0.080 20 3230969 missense variant C/G;T snv 4.0E-06; 1.2E-05 1
rs797045107 1.000 0.080 20 3234173 frameshift variant TGGCGAAGC/G delins 1