Source: UNIPROT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121918549 0.882 0.080 12 53321423 stop gained G/A;T snv 4.0E-06; 1.8E-04 1
rs1297831120 1.000 0.080 12 53314817 missense variant T/C snv 1
rs121918550 1.000 0.080 12 53309624 missense variant A/G snv 1.2E-04 4.9E-05 1
rs387906792 1.000 0.080 16 70277088 missense variant T/A snv 1
rs143370729 1.000 16 70255763 missense variant T/C snv 4.8E-05 4.2E-05 1
rs786205157 1.000 16 70277057 missense variant T/G snv 7.0E-06 1
rs387907061 1.000 6 44311507 missense variant A/C snv 1.2E-05 1.4E-05 1
rs138119149 0.807 0.280 6 44304512 missense variant G/A snv 2.1E-04 2.4E-04 1
rs587777590 1.000 6 44313175 missense variant A/C snv 1
rs587777592 1.000 6 44306367 missense variant C/T snv 1.6E-05 7.0E-06 1
rs543267101 1.000 6 44300612 missense variant C/T snv 4.0E-05 4.2E-05 1
rs1337040042 1.000 0.040 17 81131085 start lost T/C snv 1
rs121434578 1.000 0.080 16 8768248 missense variant G/A snv 1
rs189206655 1.000 0.080 9 104809521 missense variant C/T snv 4.0E-06 1.4E-05 1
rs146292819 0.790 0.240 9 104794495 missense variant T/G snv 2.9E-04 3.8E-04 1
rs137854496 1.000 0.120 9 104831048 missense variant C/A;G snv 5.6E-05; 4.0E-05 1
rs137854494 1.000 0.120 9 104806276 missense variant A/G snv 7.0E-06 1
rs137854501 1.000 0.120 9 104786940 missense variant G/A snv 7.0E-06 1
rs137854495 1.000 0.120 9 104822514 missense variant G/A snv 1.2E-05 1
rs28937314 1.000 0.120 9 104822521 missense variant T/C;G snv 1
rs137854500 1.000 0.120 9 104814154 missense variant C/T snv 2.4E-05 1
rs28937313 0.882 0.160 9 104822520 missense variant T/C snv 8.0E-06 1
rs745593394 1.000 0.120 9 104819625 missense variant G/A snv 1.2E-05 1.4E-05 1
rs137854498 1.000 0.120 9 104798504 missense variant G/A;T snv 8.0E-06; 8.0E-06 1
rs564764153 1.000 0.120 9 104785453 missense variant C/G snv 1.5E-04 1.8E-04 1