Gene: SCNN1B ×
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: 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
dbSNP: rs61759921
rs61759921
SCNN1B
1 1.000 0.040 16 23371460 missense variant G/A snv 6.0E-05 7.7E-05 0.700 0
dbSNP: rs72654338
rs72654338
SCNN1B
1 1.000 0.040 16 23367959 missense variant G/A;T snv 7.2E-05 0.700 0