Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397508635
CFTR
0.925 0.160 7 117480132 missense variant C/A;T snv 1
rs149353983
CFTR
1.000 0.120 7 117504291 missense variant G/A;T snv 5.6E-05; 3.2E-05 1
rs77284892
CFTR
0.851 0.160 7 117509047 stop gained G/A;T snv 2.4E-05 1
rs368505753
CFTR
0.925 0.160 7 117509069 missense variant C/T snv 3.6E-05 3.5E-05 1
rs115545701
CFTR
0.925 0.160 7 117509089 missense variant C/T snv 1.5E-03 4.3E-03 2
rs1800076
CFTR
0.763 0.200 7 117509093 missense variant G/A;T snv 1.5E-02; 8.0E-06 9
rs75961395
CFTR
0.763 0.280 7 117509123 missense variant G/A;T snv 4.0E-05 9
rs121908751
CFTR
0.925 0.160 7 117530899 stop gained G/A;T snv 4.0E-06 1
rs397508467
CFTR
1.000 0.120 7 117530921 missense variant C/T snv 8.0E-06 1
rs758675549
CFTR
0.925 0.200 7 117530938 missense variant A/G snv 4.0E-06 2
rs113993958
CFTR
0.882 0.200 7 117530953 missense variant G/A;C;T snv 2.0E-05; 4.0E-06 1
rs78655421
CFTR
0.716 0.240 7 117530975 missense variant G/A;C;T snv 1.5E-03; 1.2E-05 17
rs79660178
CFTR
1.000 0.120 7 117530991 stop gained T/A snv 1
rs76371115
CFTR
0.807 0.160 7 117531041 missense variant A/C;G;T snv 8.0E-06 5
rs35516286
CFTR
0.851 0.160 7 117531068 missense variant T/A;C snv 1.8E-03 3
rs397508718
CFTR
0.925 0.160 7 117531070 stop gained G/A;T snv 1
rs397508725
CFTR
1.000 0.120 7 117531098 missense variant G/A;C snv 7.2E-05; 2.0E-05 1
rs397508731
CFTR
1.000 0.120 7 117531109 missense variant A/G snv 1
rs1800080
CFTR
0.925 0.120 7 117534330 missense variant A/G snv 2
rs1396707015
CFTR
1.000 0.120 7 117535273 stop gained G/A snv 1
rs121908803
CFTR
0.925 0.160 7 117535281 missense variant C/A;T snv 4.0E-06 7.0E-06 1
rs121908752
CFTR
0.851 0.160 7 117535285 missense variant T/G snv 1.9E-04 1.3E-04 1
rs397508778
CFTR
0.851 0.160 7 117535326 stop gained C/T snv 4.0E-06 1
rs397508783
CFTR
0.925 0.160 7 117535363 missense variant T/A snv 2.4E-05 7.0E-06 1
rs397508786
CFTR
1.000 0.120 7 117535381 missense variant C/T snv 1