Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2070600
AGER
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs12252
IFITM3
0.695 0.240 11 320772 splice region variant A/G snv 0.13 0.13 23
rs315952
IL1RN
0.763 0.400 2 113132727 missense variant T/A;C snv 4.0E-06; 0.31 10
rs1965708
SFTPA2
0.851 0.200 10 79557289 missense variant G/T snv 0.22 0.25 6
rs121434431
TLR3
0.851 0.080 4 186083346 missense variant C/T snv 4.1E-04 5.2E-04 4
rs1059046
SFTPA2
0.882 0.120 10 79559458 missense variant G/C;T snv 2.2E-05; 0.46 3