Source: UNIPROT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs61751507 1.000 0.080 10 100069757 missense variant C/T snv 4.2E-02 3.4E-02 1
rs558683362 1.000 0.120 4 1000895 missense variant G/A;C snv 4.0E-06 1
rs141371306 1.000 0.080 13 100111886 missense variant C/T snv 2.0E-05 5.6E-05 1
rs374993554 0.925 7 100113899 missense variant A/G;T snv 3.2E-05 1
rs727503778 0.925 0.080 7 100114074 missense variant G/A snv 1
rs876661307 1.000 1 100123231 missense variant A/G snv 1
rs367737727
EVL
1.000 0.080 14 100128600 missense variant C/T snv 1.1E-05 1
rs992336192 1.000 0.120 4 1001506 missense variant G/A;C snv 1
rs754154200 1.000 0.120 4 1001518 missense variant G/A snv 4.0E-06 7.0E-06 1
rs202247814 1.000 0.080 13 100155090 missense variant G/A snv 1
rs1430681871 1.000 0.120 4 1001712 missense variant G/A snv 7.0E-06 1
rs1230234600 1.000 0.120 4 1001745 missense variant G/A;C snv 1
rs1333017606 1.000 0.080 7 100175622 missense variant C/G;T snv 4.0E-06; 8.0E-06 1
rs148789453 0.882 0.120 4 1001802 missense variant T/A;G snv 2.2E-05; 4.4E-06 1
rs876661322 1.000 10 100183802 missense variant C/A snv 1
rs863225072 1.000 0.160 4 10019000 missense variant A/C snv 6.5E-06 2.8E-05 1
rs369090960 1.000 0.120 4 1001982 missense variant G/A;C snv 2.1E-05; 5.2E-06 1
rs12021720
DBT
0.925 0.160 1 100206504 missense variant T/A;C snv 0.92 1
rs202247815 1.000 0.080 13 100209354 missense variant T/C snv 4.0E-06 1
rs121964999
DBT
0.882 0.120 1 100214929 missense variant A/C snv 1.1E-04 1.0E-04 1
rs199801029 0.925 0.120 4 1002275 missense variant G/C snv 6.6E-05 7.7E-05 1
rs121965001
DBT
1.000 0.120 1 100230872 missense variant G/C snv 1
rs121965033 0.925 0.120 4 1002333 missense variant T/C;G snv 4.0E-06 1
rs746766617 0.882 0.120 4 1002340 missense variant C/G snv 4.0E-06 1
rs368454909 1.000 0.120 4 1002341 missense variant G/A snv 4.0E-06 7.0E-06 1