Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs74597325
CFTR
0.708 0.320 7 117587811 stop gained C/G;T snv 6.8E-05 18
rs113993959
CFTR
0.677 0.280 7 117587778 stop gained G/A;T snv 8.0E-06; 3.4E-04 25
rs213950
CFTR-AS1 ; CFTR
0.716 0.320 7 117559479 missense variant G/A snv 0.47 0.57 16
rs4251961
IL1RN
0.763 0.200 2 113116890 intron variant T/C snv 0.29 10
rs587782477
APC
0.882 0.120 5 112775679 missense variant A/T snv 4
rs4957796
FER
0.851 0.120 5 109066439 intron variant T/C snv 0.16 5
rs7309123
LOC105369655 ; CLEC7A
0.807 0.280 12 10119994 intron variant G/C snv 0.42 8