Source: UNIPROT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121912429 1.000 0.080 15 98922162 missense variant G/A snv 1.2E-05 2.1E-05 1
rs1350566881 1.000 6 98917618 missense variant A/G snv 1
rs761168789 1.000 16 9891000 missense variant G/A snv 4.0E-06 1
rs587777729 1.000 3 9890785 missense variant G/T snv 1
rs777966677 1.000 3 9890781 missense variant G/A snv 7.0E-06 1
rs786205704 1.000 3 9890762 missense variant G/A;T snv 1
rs121908321 0.925 0.200 4 9890687 missense variant G/A;T snv 2.1E-04; 8.0E-06 1
rs1064795875 1.000 5 98902916 missense variant T/C snv 1
rs1554078856 1.000 5 98897307 missense variant C/T snv 1
rs1554078349 1.000 5 98893554 missense variant C/T snv 1
rs772037717 0.882 0.080 6 98875675 missense variant A/G snv 1.2E-05 1.4E-05 1
rs398123061 0.882 0.120 6 98875673 missense variant G/A snv 2.8E-05 2.8E-05 1
rs1554215979 1.000 6 98875465 missense variant A/T snv 1
rs201989042 1.000 6 98874354 missense variant T/G snv 2.0E-05 1.4E-05 1
rs1293161341 1.000 5 98856390 missense variant C/T snv 1
rs267606840 1.000 9 98845990 missense variant C/A;T snv 4.0E-06 1
rs1272530441 1.000 9 98837123 missense variant A/G snv 7.0E-06 1
rs868590153 1.000 9 98837081 missense variant G/A;C;T snv 2.4E-05 1
rs920049418 1.000 9 98837054 missense variant G/A snv 4.2E-05 1
rs145236923 0.851 0.120 9 98831947 missense variant G/A snv 1.2E-03 1.3E-03 1
rs149726976 0.882 0.120 9 98831929 missense variant C/T snv 2.7E-04 4.5E-04 1
rs121965029 0.851 0.120 4 987916 missense variant G/A snv 9.2E-06 7.0E-06 1
rs754966840 0.925 0.120 4 987915 missense variant C/T snv 1.4E-05 1
rs794727239 1.000 0.120 4 987895 missense variant A/C snv 4.2E-06 7.0E-06 1
rs747981483 1.000 0.120 4 987886 missense variant C/T snv 4.2E-06 1