Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121434287 1.000 0.080 8 144415295 missense variant G/A snv 1.3E-04 1.4E-04 1
rs121434288 1.000 0.080 8 144413288 missense variant C/T snv 1
rs121434289 1.000 0.080 8 144414291 missense variant C/T snv 2.1E-05 2.1E-05 1
rs121434290 1.000 0.080 8 144415966 missense variant G/T snv 1
rs121434291 1.000 0.080 8 144414422 missense variant C/T snv 1
rs121434293 1.000 0.080 8 144414792 missense variant C/G snv 1
rs1871534 1.000 0.080 8 144414297 missense variant C/G snv 0.76 1
rs2977838 1.000 0.080 8 144415027 missense variant G/A snv 3.2E-02 1
rs782110796 1.000 0.080 8 144414775 missense variant C/T snv 8.0E-06 1
rs121434292 0.925 0.120 8 144416001 missense variant G/A;T snv 9.9E-06 2
rs534850657 0.925 0.120 8 144413980 missense variant A/G snv 2
rs782427403 0.925 0.120 8 144413980 frameshift variant A/- del 4.2E-06 7.0E-06 2