Source: UNIPROT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs372066126 1.000 0.040 1 9975681 missense variant A/G snv 8.0E-06 2.1E-05 1
rs756903689 1.000 0.040 1 9975675 missense variant G/T snv 1.2E-05 7.0E-06 1
rs763325435 0.925 0.040 1 9975672 missense variant C/T snv 4.0E-06; 8.4E-05 2.1E-05 1
rs760965874 1.000 0.040 1 9975637 missense variant C/T snv 1.2E-05 7.0E-06 1
rs28939711 0.851 0.120 10 99724057 missense variant G/A snv 3.2E-05 3.5E-05 2
rs761948762 1.000 0.040 1 9972132 missense variant T/A snv 4.0E-06 1
rs138613460 1.000 0.040 1 9972110 missense variant G/A snv 1.6E-04 5.6E-04 1
rs386834104 1.000 0.320 8 99720944 missense variant A/G snv 4.0E-06 1.4E-05 1
rs120074149 1.000 0.320 8 99717219 missense variant T/G snv 1
rs397514662 0.882 0.120 10 99716419 missense variant A/C;G snv 1.2E-05 1
rs199422221 1.000 0.080 4 99619094 missense variant A/T snv 1
rs767833468 1.000 0.080 4 99618993 missense variant G/A snv 4.0E-06 1
rs199422222 1.000 0.080 4 99608977 missense variant G/T snv 1
rs199422220 1.000 0.080 4 99608827 missense variant G/A snv 1.6E-05 3.5E-05 1
rs372321643 1.000 0.080 4 99608826 missense variant C/T snv 2.8E-05 4.2E-05 1
rs1485375137 1.000 0.080 4 99608790 missense variant T/C snv 7.0E-06 1
rs1367079155 1.000 0.080 4 99594764 missense variant G/C snv 4.0E-06 1
rs587777744 1.000 4 99553814 missense variant C/T snv 1
rs28942091 1.000 3 9943452 missense variant C/G;T snv 6.5E-04 1
rs28942092 1.000 3 9943399 stop gained C/T snv 5.0E-04 5.4E-04 1
rs121912626 1.000 3 9940873 missense variant C/G snv 1
rs147238850 1.000 7 99391182 missense variant G/A snv 1.4E-04 1.7E-04 1
rs199528312 1.000 16 9938097 missense variant G/A snv 3.6E-05 1.4E-05 1
rs28941780 0.925 0.120 3 9937624 missense variant G/A snv 3.5E-04 1.4E-03 1
rs1033602309 1.000 0.080 X 9937279 missense variant G/C snv 1