Source: UNIPROT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1466524306 1.000 0.040 13 99295133 missense variant G/A snv 4.0E-06 1
rs750610248 0.882 0.200 14 99175513 missense variant A/C;G snv 4.1E-06 1
rs786205156 1.000 2 99162492 missense variant A/G snv 4.0E-06 1
rs137973334 1.000 2 99162249 missense variant C/G;T snv 1.2E-04; 4.0E-06 1
rs767568897 1.000 2 99162169 missense variant C/G;T snv 8.0E-06; 8.8E-05 1
rs142573758 1.000 0.080 4 991538 missense variant C/T snv 5.6E-04 6.0E-04 1
rs113605875 0.882 0.120 9 99149253 missense variant G/A;C;T snv 1
rs111426349 0.882 0.120 9 99149252 missense variant C/A;T snv 4.0E-06 1
rs121918711 1.000 0.120 9 99146553 missense variant A/G snv 1
rs121918710 1.000 0.120 9 99142683 missense variant T/G snv 1
rs111854391 0.716 0.280 9 99138006 stop gained C/A;T snv 4.0E-06 1
rs121918712 1.000 0.120 9 99137883 missense variant C/T snv 1
rs757374917 9 99129005 missense variant C/T snv 1
rs587776865 9 99128911 missense variant G/C snv 1
rs387906696 9 99128891 missense variant A/G snv 8.0E-06 2.8E-05 1
rs139024319 1.000 0.080 4 991150 missense variant G/A snv 2.5E-04 1.6E-04 1
rs148832260 1.000 0.080 4 989866 missense variant G/A snv 2.8E-04 3.1E-04 1
rs1294404368 1.000 0.080 7 98981947 missense variant C/T snv 4.4E-06 1.4E-05 1
rs753661271 1.000 0.080 7 98976613 missense variant C/T snv 4.0E-06 1
rs528967912 1.000 0.080 7 98964724 missense variant C/T snv 1.6E-05 7.0E-06 1
rs141802822 1.000 0.080 15 98957347 missense variant C/T snv 3.3E-04 6.8E-04 1
rs782203759 1.000 0.080 7 98950120 missense variant G/A snv 2.4E-05 2.8E-05 1
rs373632999 1.000 0.080 7 98949733 missense variant G/A snv 1.2E-05 4.2E-05 1
rs587777730 1.000 3 9893310 missense variant A/G snv 8.0E-06 1.4E-05 1
rs587777728 1.000 3 9892955 missense variant C/T snv 1