Source: UNIPROT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057520384
TH
1.000 0.040 11 2166003 missense variant G/A;T snv 5.9E-06; 5.9E-06 1
rs121917762
TH
0.925 0.040 11 2165727 stop gained G/A;T snv 4.0E-06; 4.0E-06 1
rs121917763
TH
0.925 0.040 11 2167896 missense variant A/G snv 1.2E-05 7.0E-06 1
rs121917764
TH
1.000 0.040 11 2166762 missense variant G/A;C snv 7.0E-06 1
rs121917765
TH
1.000 0.040 11 2166544 missense variant C/A snv 1
rs1264884607
TH
1.000 0.040 11 2165679 missense variant C/T snv 2.0E-05 2.1E-05 1
rs1273610334
TH
1.000 0.040 11 2166985 missense variant C/A snv 4.8E-06 1
rs1288483479
TH
1.000 0.040 11 2166760 missense variant C/T snv 7.0E-06 1
rs1428589694
TH
1.000 0.040 11 2166721 missense variant G/A snv 1
rs1554922725
TH
1.000 0.040 11 2166054 missense variant A/G snv 1
rs199961079
TH
1.000 0.040 11 2166934 missense variant C/T snv 3.1E-05 3.5E-05 1
rs28934580
TH
1.000 0.040 11 2166693 missense variant C/T snv 1
rs28934581
TH
1.000 0.040 11 2166995 missense variant T/G snv 1.5E-05 1
rs367874223
TH
0.925 0.040 11 2165337 missense variant C/G;T snv 2.4E-05 1
rs370962049
TH
1.000 0.040 11 2165721 missense variant C/A;T snv 8.0E-06; 1.6E-05 1
rs45471299
TH
1.000 0.040 11 2164339 missense variant G/A snv 4.0E-05 2.1E-05 1
rs745551241
TH
1.000 0.040 11 2165739 missense variant C/G;T snv 4.0E-06 1
rs755536257
TH
1.000 0.040 11 2166941 missense variant C/A;G;T snv 1.8E-05 1
rs762304556
TH
1.000 0.040 11 2167484 missense variant C/G;T snv 6.6E-05 1
rs763039181
TH
1.000 0.040 11 2166045 missense variant G/A snv 1.8E-05 1
rs763198914
TH
1.000 0.040 11 2166495 missense variant G/A;C snv 4.7E-06; 4.7E-06 1
rs80338892
TH
1.000 0.040 11 2167905 missense variant C/T snv 1.1E-04 1.4E-04 1