Source: UNIPROT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs373921680
HGD
1.000 0.080 3 120674952 missense variant T/G snv 4.4E-05 7.0E-05 1
rs756134838
HGD
1.000 0.080 3 120647015 missense variant A/C snv 8.0E-06 1
rs120074171
HGD
1.000 0.080 3 120638471 missense variant C/A;G;T snv 2.4E-05 1
rs1458752246
HGD
1.000 0.080 3 120675842 start lost C/T snv 4.0E-06 7.0E-06 1
rs120074172
HGD
1.000 0.080 3 120633223 missense variant T/C snv 3.6E-05; 4.0E-06 1.2E-04 1
rs200808744
HGD
1.000 0.080 3 120674919 missense variant C/T snv 4.0E-05 5.6E-05 1
rs368717991
HGD
1.000 0.080 3 120633257 missense variant C/G snv 1.2E-05 1.4E-05 1
rs120074170
HGD
1.000 0.080 3 120638562 missense variant A/C;G snv 1
rs1414279737
HGD
1.000 0.080 3 120646327 missense variant T/C snv 4.0E-06 1.4E-05 1
rs1553717936
HGD
1.000 0.080 3 120647891 missense variant C/G snv 1
rs755734596
HGD
1.000 0.080 3 120650865 missense variant C/G snv 8.0E-06 7.0E-06 1
rs564979861
HGD
1.000 0.080 3 120650841 missense variant C/T snv 2.4E-05 2.1E-05 1
rs375283568
HGD
1.000 0.080 3 120647020 missense variant C/T snv 1.6E-05 4.2E-05 1
rs1174584850
HGD
1.000 0.080 3 120670524 missense variant T/C snv 7.0E-06 1
rs752153829
HGD
1.000 0.080 3 120650849 missense variant C/A;T snv 3.6E-05; 4.0E-06 1
rs759843592
HGD
1.000 0.080 3 120644320 missense variant T/G snv 1
rs28941783
HGD
1.000 0.080 3 120647041 missense variant C/T snv 8.8E-05 1.6E-04 1
rs1349543050
HGD
1.000 0.080 3 120646974 missense variant T/C snv 4.0E-06 1
rs120074173
HGD
1.000 0.080 3 120633233 missense variant T/C snv 1.7E-04 3.0E-04 1
rs767201131
HGD
1.000 0.080 3 120646269 missense variant A/G snv 4.0E-06 1
rs138558042
HGD
1.000 0.080 3 120633217 missense variant G/A snv 7.0E-06 1
rs1160502581
HGD
1.000 0.080 3 120641640 missense variant C/G;T snv 4.0E-06 1
rs754428438
HGD
1.000 0.080 3 120641595 missense variant G/A;T snv 4.0E-06; 8.0E-06 1
rs1324654414
HGD
1.000 0.080 3 120670527 missense variant A/G snv 4.0E-06 7.0E-06 1
rs377498269 1.000 0.080 11 121558698 missense variant A/G snv 4.0E-05 4.2E-05 1