Source: UNIPROT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397508363
CFTR
1.000 0.040 7 117592464 missense variant G/A;C;T snv 4.5E-06 1
rs397508448
CFTR
1.000 0.040 7 117603750 missense variant C/T snv 8.0E-06 7.0E-06 1
rs397508241
CFTR
1.000 0.040 7 117587785 missense variant G/T snv 1
rs397508373
CFTR
1.000 0.040 7 117592566 missense variant C/G;T snv 5.5E-06 1
rs397508220
CFTR
1.000 0.040 7 117504348 missense variant C/A snv 7.0E-06 1
rs193922511
CFTR
1.000 0.040 7 117603687 missense variant T/G snv 1.6E-05 2.8E-05 1
rs397508567
CFTR
1.000 0.040 7 117614703 missense variant T/A snv 3.2E-05 2.8E-05 1
rs1800098
CFTR
1.000 0.040 7 117590400 missense variant G/C;T snv 5.1E-03; 4.0E-06 1
rs397508670
CFTR
1.000 0.040 7 117664815 missense variant C/T snv 3.6E-05 2.8E-05 1
rs397508790
CFTR
1.000 0.040 7 117535399 missense variant T/A snv 1
rs140502196
CFTR
1.000 0.040 7 117530957 missense variant C/G;T snv 6.0E-05 1
rs397508195
CFTR ; CFTR-AS1
1.000 0.120 7 117548797 missense variant G/C;T snv 1
rs397508315
CFTR
1.000 0.120 7 117592027 missense variant T/G snv 1
rs150691494
CFTR
1.000 0.120 7 117540132 missense variant A/G snv 2.9E-04 1.8E-04 1
rs77902683
CFTR
1.000 0.120 7 117642568 missense variant G/A;T snv 4.0E-06 1
rs193922504
CFTR
1.000 0.120 7 117587827 missense variant T/C snv 4.0E-06 7.0E-06 1
rs397508314
CFTR
1.000 0.120 7 117592026 missense variant A/C;G;T snv 8.6E-06; 4.3E-06 1
rs397508621
CFTR
1.000 0.120 7 117642592 missense variant A/G snv 4.0E-06 1
rs121909016
CFTR
1.000 0.120 7 117540163 missense variant C/G snv 1
rs397508282
CFTR
1.000 0.120 7 117590387 missense variant G/A snv 1
rs397508146
CFTR
1.000 0.120 7 117540267 missense variant T/C snv 1
rs397508280
CFTR
1.000 0.120 7 117590385 missense variant T/C snv 1
rs201978662
CFTR
1.000 0.120 7 117592004 missense variant G/A snv 7.0E-06 1
rs397508819
CFTR
1.000 0.120 7 117540170 missense variant G/C;T snv 1
rs121909020
CFTR
1.000 0.120 7 117611640 missense variant G/A;C snv 4.0E-06 1