Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs592297
PICALM
0.925 0.080 11 86014894 synonymous variant C/T snv 0.78 0.82 2
rs11234495
PICALM
1.000 0.080 11 85964391 intron variant C/T snv 0.23 1
rs588076
PICALM
1.000 0.080 11 85980619 intron variant G/A;C snv 1
rs676733
PICALM
1.000 0.080 11 86022967 intron variant C/T snv 0.72 1
rs677909
PICALM
1.000 0.080 11 86046547 intron variant C/T snv 0.72 1