Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs58072617
KRT5
0.790 0.120 12 52517702 missense variant A/G;T snv 7
rs59115483
KRT5
0.882 0.080 12 52519789 missense variant C/T snv 2.4E-05 7.0E-06 4
rs59190510
KRT5
0.851 0.080 12 52516647 stop gained C/A;T snv 4
rs762236241
GALK1 ; ITGB4
0.882 0.080 17 75757312 splice donor variant T/C snv 2.0E-05 3
rs58762773
KRT14
0.882 0.080 17 41583245 missense variant C/G;T snv 4.0E-06 3
rs59966597
KRT14
1.000 0.080 17 41583347 missense variant G/A;C snv 4.0E-06 3
rs61027685
KRT14
0.882 0.080 17 41586438 missense variant C/A;G;T snv 3
rs60586163
KRT5
0.882 0.080 12 52519137 missense variant G/A;C;T snv 4.0E-06 3
rs57358989
KRT14
0.925 0.080 17 41586478 missense variant C/T snv 2
rs61263401
KRT14
0.925 0.080 17 41586480 missense variant T/C snv 2
rs57142010
KRT5
0.925 0.080 12 52517699 missense variant T/A;C snv 2
rs58766676
KRT5
0.925 0.080 12 52519120 missense variant T/A;C;G snv 2
rs59464425
KRT5
0.925 0.080 12 52517698 missense variant G/A;T snv 2
rs61222761
KRT5
0.925 0.080 12 52519824 missense variant T/A snv 2
rs61495052
KRT5
0.925 0.080 12 52519767 missense variant T/C snv 2
rs56974573
KRT14
1.000 0.080 17 41583384 inframe deletion CCT/- delins 1
rs57200223
KRT14
1.000 0.080 17 41583287 missense variant G/A;T snv 1.6E-05 1
rs58378809
KRT14
1.000 0.080 17 41586393 missense variant G/A;C snv 4.0E-06 1
rs58560979
KRT14
1.000 0.080 17 41583879 missense variant C/T snv 1
rs58645163
KRT14
1.000 0.080 17 41583346 missense variant C/G;T snv 1.5E-04 1
rs58785777
KRT14
1.000 0.080 17 41583866 missense variant G/T snv 1
rs59271739
KRT14
1.000 0.080 17 41586487 missense variant C/G;T snv 4.0E-06 1
rs59375065
KRT14
1.000 0.080 17 41583869 missense variant T/C snv 1
rs59442925
KRT14
1.000 0.080 17 41583265 missense variant T/C snv 1
rs60589227
KRT14
1.000 0.080 17 41584390 missense variant C/A;G;T snv 3.2E-05; 1.6E-05 1