Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17235409
SLC11A1
0.653 0.600 2 218395009 missense variant G/A;C snv 4.9E-02; 4.1E-06 31
rs2069705
IFNG-AS1 ; IFNG
0.695 0.440 12 68161231 intron variant G/A;C snv 19
rs1333955
PACRG
0.851 0.080 6 162792422 intron variant T/A;C snv 4
rs9282799
NOS2
1.000 0.080 17 27801702 intron variant G/A snv 1.5E-02 1