Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs147680216
WNT10A
0.742 0.160 2 218890244 missense variant G/A snv 2.1E-03 6.9E-04 11
rs144078282
CLPB
0.776 0.400 11 72302339 missense variant T/A;C snv 1.8E-04; 2.0E-04 9
rs200203460
CLPB
0.776 0.400 11 72302312 stop gained G/A;C;T snv 2.8E-05 9
rs1173679499
TP63
0.827 0.280 3 189869372 missense variant G/A snv 4.0E-06 5
rs132630321
EDA
0.851 0.120 X 70035446 missense variant C/T snv 5.5E-06 9.6E-06 4
rs1033252267
CD28
0.882 0.200 2 203729681 missense variant G/T snv 3
rs137853327
IKBKG
0.882 0.160 X 154564418 missense variant A/T snv 3
rs104894281
NECTIN1
0.882 0.320 11 119677734 stop gained C/T snv 3
rs387907197
EDA
0.925 0.080 X 70033430 missense variant C/T snv 2
rs28933100
NFKBIA
0.925 0.120 14 35404550 missense variant C/A;T snv 2
rs1553275192
PKP1
0.925 0.080 1 201316692 stop gained C/T snv 2
rs1553445945
EDAR ; RANBP2
1.000 0.080 2 108912677 splice donor variant C/T snv 1
rs56240927
FGFR3
1.000 0.080 4 1804906 missense variant C/T snv 1.3E-03 8.2E-04 1
rs4797100
MYOM1
1.000 0.080 18 3138555 intron variant A/G snv 0.25 1
rs763088741
PAX9
1.000 0.080 14 36676439 missense variant C/T snv 4.0E-06 1
rs9284390
ROCK1P1 ; MIR8078
1.000 0.080 18 112535 non coding transcript exon variant G/A;C;T snv 1