Source: UNIPROT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1000990130 1.000 0.120 12 76346999 missense variant G/A snv 7.0E-06 1
rs1003158162 1.000 0.080 2 178531968 missense variant G/A snv 4.0E-06 1
rs1003611285 1.000 0.120 19 12893590 missense variant G/A;T snv 7.0E-06 1
rs1004881058 1.000 0.080 20 1980471 missense variant C/T snv 8.0E-06 7.0E-06 1
rs1005687078 1.000 0.080 11 64753928 missense variant A/G snv 2.8E-05 1
rs1006158872
MPL
1.000 0.080 1 43346931 missense variant G/C snv 4.0E-06 7.0E-06 1
rs1007859875 1.000 0.160 11 119092137 missense variant G/A snv 4.0E-06 1.4E-05 1
rs1008642 0.882 0.120 3 8733975 missense variant C/A;G;T snv 0.29 1
rs1010372555 1.000 15 89318712 missense variant G/A;C snv 4.0E-06; 4.0E-06 1
rs1010907740 1.000 8 144084471 missense variant T/C snv 1
rs1010930015 1.000 0.040 12 64460250 missense variant A/C snv 4.2E-06 1
rs1011539285 1.000 15 44669391 missense variant A/G snv 6.5E-06 1
rs10127939 0.851 0.160 1 161548543 missense variant A/C;T snv 4.3E-02; 5.5E-02 1
rs1012947103 1.000 0.080 20 3912505 missense variant G/A snv 7.0E-06 1
rs1014317450 1.000 17 78997112 missense variant T/A snv 1.2E-05 1
rs1014369151 1.000 13 27623014 missense variant C/T snv 1
rs1014551540 1.000 0.120 17 3489247 missense variant G/T snv 1.4E-05 1
rs1015051007 1.000 0.120 2 210612273 missense variant C/A;T snv 1.2E-05 1
rs10151259 1.000 0.080 14 21321881 missense variant G/T snv 0.20 0.22 1
rs1016604233 1.000 0.080 7 139911241 missense variant C/T snv 8.0E-06 2.1E-05 1
rs1017946059
EVC
0.925 0.160 4 5731657 missense variant G/A snv 8.1E-06 7.0E-06 1
rs1018084204 0.925 0.080 8 27463317 missense variant G/A snv 4.0E-06 1
rs1020175890 1.000 0.040 2 222221362 missense variant C/T snv 1
rs1021330566 1.000 16 23544679 missense variant C/T snv 7.0E-06 1
rs1021988376 1.000 0.040 7 87453103 missense variant C/T snv 1