Disease: Flatfoot
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
rs1554888939
EHMT1
0.683 0.640 9 137798823 missense variant G/T snv 58
rs1569509136
HUWE1
0.708 0.400 X 53647576 splice acceptor variant T/C snv 24
rs879253753
ANKRD11
0.851 0.280 16 89280526 frameshift variant -/T delins 19