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
rs60399023
KRT14
0.827 0.200 17 41586462 missense variant G/A;C snv 5
rs58330629
KRT14
0.851 0.120 17 41586461 missense variant C/A;G;T snv 4
rs59190510
KRT5
0.851 0.080 12 52516647 stop gained C/A;T snv 4
rs28928893
KRT14
0.882 0.120 17 41586479 missense variant A/G snv 3
rs58762773
KRT14
0.882 0.080 17 41583245 missense variant C/G;T snv 4.0E-06 3
rs60586163
KRT5
0.882 0.080 12 52519137 missense variant G/A;C;T snv 4.0E-06 3
rs58380626
KRT14
0.925 0.080 17 41583266 missense variant A/G snv 2
rs59110575
KRT14
0.925 0.080 17 41586471 missense variant G/A snv 2
rs60171927
KRT14
0.925 0.080 17 41586467 missense variant T/C snv 2
rs60470268
KRT14
0.925 0.080 17 41586450 missense variant A/C snv 2
rs60715293
KRT5
0.925 0.080 12 52519756 missense variant A/G snv 2
rs61348633
KRT5
0.925 0.080 12 52516652 missense variant T/C snv 2
rs3826549
KRT14
1.000 0.080 17 41586466 missense variant A/G;T snv 0.64 1
rs57364972
KRT14
1.000 0.080 17 41583253 missense variant A/T snv 1
rs57522245
KRT14
1.000 0.080 17 41586446 missense variant A/G snv 1
rs60622724
KRT14
1.000 0.080 17 41583262 missense variant C/A;G;T snv 4.0E-06; 6.0E-05 1
rs60993843
KRT14
1.000 0.080 17 41586476 missense variant T/C;G snv 1
rs61085704
KRT14
1.000 0.080 17 41583259 missense variant C/A;G;T snv 4.0E-06; 4.4E-05 1
rs267607456
KRT5
1.000 0.080 12 52519802 missense variant C/A;G snv 1
rs57155193
KRT5
1.000 0.080 12 52516653 missense variant C/T snv 1
rs57781042
KRT5
1.000 0.080 12 52519761 missense variant A/G snv 1
rs57890479
KRT5
1.000 0.080 12 52519774 missense variant G/A snv 1
rs58619430
KRT5
1.000 0.080 12 52519795 missense variant C/T snv 1
rs59092197
KRT5
1.000 0.080 12 52519770 missense variant T/C snv 1