Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs368869806
PTCH1
0.614 0.480 9 95485875 splice acceptor variant C/T snv 4.0E-06 7.0E-06 97
rs1555462347
USP7
0.716 0.520 16 8901028 frameshift variant CT/- delins 34
rs1064795559
MORC2
0.752 0.320 22 30946373 missense variant G/A snv 29