Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs77284892
rs77284892
CFTR
4 0.851 0.160 7 117509047 stop gained G/A;T snv 2.4E-05 0.700 0
dbSNP: rs77834169
rs77834169
CFTR
4 0.851 0.160 7 117530974 missense variant C/A;G;T snv 8.0E-06; 2.0E-05; 2.0E-04 0.700 0
dbSNP: rs78655421
rs78655421
CFTR
18 0.716 0.240 7 117530975 missense variant G/A;C;T snv 1.5E-03; 1.2E-05 0.700 0
dbSNP: rs78756941
rs78756941
CFTR
4 0.851 0.160 7 117531115 splice donor variant G/T snv 7.7E-05 1.0E-04 0.700 0
dbSNP: rs78802634
rs78802634
CFTR
4 0.851 0.160 7 117611707 stop gained G/A snv 2.4E-05 0.700 0
dbSNP: rs79850223
rs79850223
CFTR
4 0.851 0.160 7 117627525 stop gained C/T snv 3.2E-05 2.8E-05 0.700 0
dbSNP: rs80224560
rs80224560
CFTR
4 0.851 0.160 7 117602868 splice region variant G/A snv 7.6E-05 6.3E-05 0.700 0
dbSNP: rs80282562
rs80282562
CFTR
4 0.851 0.160 7 117534318 missense variant G/A snv 1.6E-05 0.700 0
dbSNP: rs137852709
rs137852709
SCNN1B
1 1.000 0.040 16 23367879 missense variant C/T snv 0.800 1.000 3 2005 2009
dbSNP: rs137852710
rs137852710
SCNN1B
1 1.000 0.040 16 23380493 missense variant G/A snv 8.0E-06 7.0E-06 0.800 1.000 3 2005 2009
dbSNP: rs137852711
rs137852711
SCNN1B
1 1.000 0.040 16 23371836 missense variant C/A snv 4.4E-05 1.3E-04 0.800 1.000 3 2005 2009
dbSNP: rs137852712
rs137852712
SCNN1B
1 1.000 0.040 16 23367942 missense variant A/G snv 8.0E-06 0.800 1.000 3 2005 2009
dbSNP: rs35731153
rs35731153
SCNN1B
1 1.000 0.040 16 23348844 missense variant C/G snv 4.8E-03 4.6E-03 0.800 1.000 3 2005 2009