Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1064794254
UPF3B
0.851 0.120 X 119841185 frameshift variant CT/- delins 6
rs1564421528
WAC
0.882 0.080 10 28614666 stop gained C/T snv 16
rs1567010427
DYNC1H1
0.882 14 102010824 missense variant G/A snv 11
rs542652468
ATP1A3
0.882 19 41986177 missense variant G/A;T snv 6
rs1057518864
TCF4
0.925 18 55350409 splice acceptor variant C/T snv 7