Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs387906905
TRPV4
0.882 0.120 12 109798819 missense variant C/T snv 10
rs137854521
ANO5
0.851 0.200 11 22221100 frameshift variant -/A delins 9
rs1555452876
PKD1 ; MIR6511B1
1.000 16 2106222 inframe deletion CTC/- delins 5
rs118192174
RYR1
0.882 0.200 19 38499961 missense variant T/A snv 2.0E-05 2.1E-05 5