Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1130866
SFTPB
0.827 0.160 2 85666618 missense variant G/A;C snv 0.50 9
rs2249825
HMGB1
0.695 0.440 13 30463766 5 prime UTR variant G/A;C;T snv 23
rs113993959
CFTR
0.677 0.280 7 117587778 stop gained G/A;T snv 8.0E-06; 3.4E-04 25
rs7309123
LOC105369655 ; CLEC7A
0.807 0.280 12 10119994 intron variant G/C snv 0.42 8
rs2294021
CCDC22
0.776 0.280 X 49249149 intron variant T/A;C snv 0.52 8
rs4308977
CR2
0.925 0.160 1 207473553 missense variant T/A;C snv 4.0E-06; 0.27 2
rs4251961
IL1RN
0.763 0.200 2 113116890 intron variant T/C snv 0.29 10
rs4957796
FER
0.851 0.120 5 109066439 intron variant T/C snv 0.16 5