Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121434421
PKP2
0.925 0.080 12 32802499 stop gained G/A;C snv 4.0E-06; 4.0E-06; 1.6E-05 2
rs121913006
DSG2
0.925 0.080 18 31519867 missense variant G/A snv 4.0E-06 2
rs121913008
DSG2
0.925 0.080 18 31519858 missense variant G/A snv 7.0E-06 2
rs121913010
DSG2 ; DSG2-AS1
0.925 0.080 18 31545820 missense variant G/A;C;T snv 2.4E-05; 1.2E-05 2
rs144601090
PKP2
0.925 0.080 12 32821439 missense variant A/G snv 1.6E-05 1.1E-04 2
rs145476705
DSC2
0.925 0.080 18 31087781 stop gained A/G;T snv 4.0E-06; 4.0E-06 2
rs1554105614
DSP
1.000 0.080 6 7555773 stop gained C/T snv 2
rs191564916
DSG2
0.925 0.080 18 31524877 missense variant A/G snv 5.2E-04 5.9E-04 2
rs193922672
PKP2
0.925 0.080 12 32841103 stop gained C/T snv 1.6E-05 2
rs372827156
PKP2
0.925 0.080 12 32850907 stop gained G/A snv 1.2E-05 4.9E-05 2
rs397514038
DSG2
0.925 0.080 18 31541191 splice acceptor variant A/G snv 2
rs397516709
DSG2
0.925 0.080 18 31521245 splice donor variant T/C snv 8.4E-06 2
rs397516986
PKP2
0.925 0.080 12 32868965 stop gained G/A snv 4.0E-06 7.0E-06 2
rs397516990
PKP2
0.925 0.080 12 32850873 missense variant A/G snv 2
rs397517003
PKP2
0.925 0.080 12 32841027 splice donor variant C/T snv 4.0E-06 2
rs397517012
PKP2
0.925 0.080 12 32822526 stop gained G/A snv 4.0E-06 7.0E-06 2
rs41272699
DES
0.925 0.160 2 219420154 missense variant C/T snv 9.2E-03 1.0E-02 2
rs727503001
DSP
1.000 0.080 6 7579820 stop gained T/A snv 2
rs766209297
PKP2
0.925 0.080 12 32868935 missense variant G/A;C snv 4.0E-06; 4.0E-06 2
rs786204389
PKP2
0.925 0.080 12 32878545 splice acceptor variant T/A snv 2
rs794729098
PKP2
0.925 0.080 12 32796212 missense variant A/G snv 4.0E-06 2
rs869025395
DSP
0.925 0.080 6 7583113 stop gained C/T snv 2
rs1030380990
PKP2
1.000 0.080 12 32878926 missense variant C/T snv 1
rs1238227166
DSP
1.000 0.080 6 7565500 stop gained C/G;T snv 4.0E-06 1
rs1371251333
DSP
1.000 0.080 6 7568578 missense variant A/G snv 1