Source: UNIPROT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104894853
IDS
1.000 0.160 X 149490322 missense variant G/A snv 1
rs104894856
IDS
1.000 0.160 X 149500977 missense variant G/C;T snv 1
rs104894861
IDS
1.000 0.160 X 149503326 missense variant T/C snv 1
rs1085308006
IDS
1.000 0.160 X 149496419 missense variant T/A snv 1
rs113993946
IDS
0.925 0.160 X 149482996 missense variant C/A;G;T snv 1
rs113993949
IDS
1.000 0.160 X 149503477 missense variant C/T snv 1
rs113993954
IDS
1.000 0.160 X 149504185 missense variant C/T snv 1
rs145807417
IDS
1.000 0.160 X 149490395 missense variant T/C snv 1.3E-03 4.8E-03 1
rs146458524
IDS
1.000 0.160 X 149496471 missense variant C/A;T snv 1.6E-05; 3.1E-03 1
rs1557340280
IDS
1.000 0.160 X 149503473 missense variant G/A snv 1
rs193302905
IDS
1.000 0.160 X 149498129 missense variant T/C snv 1
rs193302909
IDS
1.000 0.160 X 149504210 missense variant T/C snv 1
rs193302911
IDS
1.000 0.160 X 149503371 missense variant G/T snv 1
rs199422228
IDS
1.000 0.160 X 149482894 missense variant C/G snv 1
rs199422229
IDS
1.000 0.160 X 149483135 missense variant A/C snv 1
rs199422231
IDS
0.925 0.160 X 149482997 missense variant G/A snv 1
rs201048643
IDS
1.000 0.160 X 149490383 missense variant G/A snv 9.8E-05 5.7E-05 1
rs398123249
IDS
1.000 0.160 X 149503468 missense variant G/A snv 1
rs398123250
IDS
1.000 0.160 X 149498228 missense variant A/G snv 1
rs864622773
IDS
1.000 0.160 X 149482966 missense variant T/C snv 1
rs864622779
IDS
1.000 0.160 X 149498202 missense variant C/G snv 1