Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4858647 0.925 0.080 3 24749884 intron variant C/A;G;T snv 2
rs201478192
KIDINS220
0.790 0.200 2 8731667 missense variant C/A snv 2.4E-04 2.6E-04 12
rs879255237
VPS45
0.807 0.160 1 150077763 missense variant C/A snv 7
rs318699
RGL3
0.882 0.080 19 11390564 intron variant A/G snv 0.73 3