Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1557055311
ABCD1
0.882 0.200 X 153743220 splice acceptor variant G/A;C snv 5
rs587777840
NLRC4
0.882 0.080 2 32250855 missense variant T/A snv 4
rs104895223
TNFRSF1A
0.882 0.240 12 6334108 missense variant C/A;G;T snv 4.0E-06 4
rs1450500
GRID2
1.000 0.200 4 92558124 intron variant A/G snv 0.69 2