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
rs1057521737
EP300
0.827 0.240 22 41173768 missense variant T/C snv 11
rs797045164
KIF1A
0.851 0.120 2 240785063 missense variant G/A snv 8