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: rs199473620
rs199473620
SCN5A
2 1.000 0.080 3 38554372 stop gained C/A;T snv 0.800 1.000 25 1998 2017
dbSNP: rs199473637
rs199473637
SCN5A
1 1.000 0.080 3 38550569 missense variant C/T snv 2.8E-05 1.4E-05 0.700 1.000 25 1998 2017
dbSNP: rs28937318
rs28937318
SCN5A
2 0.925 0.080 3 38606709 missense variant C/A;T snv 0.800 1.000 25 1998 2017
dbSNP: rs137854602
rs137854602
SCN5A
5 0.925 0.080 3 38555664 missense variant G/A snv 5.6E-05 1.4E-05 0.800 1.000 24 1998 2017
dbSNP: rs199473083
rs199473083
SCN5A
2 0.925 0.080 3 38609823 missense variant C/T snv 1.6E-05 0.800 1.000 24 1998 2017
dbSNP: rs199473171
rs199473171
SCN5A
1 1.000 0.080 3 38585801 missense variant G/A snv 4.0E-06 7.0E-06 0.800 1.000 24 1998 2017
dbSNP: rs199473207
rs199473207
SCN5A
3 0.882 0.120 3 38566555 missense variant G/A snv 0.700 1.000 24 1998 2017
dbSNP: rs199473565
rs199473565
SCN5A
3 0.882 0.120 3 38606743 missense variant C/T snv 4.0E-06 7.0E-06 0.800 1.000 24 1998 2017
dbSNP: rs137854600
rs137854600
SCN5A
6 0.807 0.120 3 38551504 missense variant C/A;T snv 0.700 1.000 21 1998 2016
dbSNP: rs137854609
rs137854609
SCN5A
3 0.882 0.120 3 38581170 missense variant C/A;T snv 7.9E-05 0.700 1.000 21 1998 2016
dbSNP: rs137854615
rs137854615
SCN5A
4 0.851 0.120 3 38550989 missense variant A/G snv 0.800 1.000 21 1998 2016
dbSNP: rs137854616
rs137854616
SCN5A
1 1.000 0.080 3 38566465 missense variant C/T snv 2.8E-05 7.0E-06 0.700 1.000 21 1998 2016
dbSNP: rs137854617
rs137854617
SCN5A
3 0.882 0.120 3 38581002 stop gained C/A;T snv 1.1E-04 1.5E-04 0.800 1.000 21 1998 2016
dbSNP: rs137854618
rs137854618
SCN5A
15 0.742 0.120 3 38566426 missense variant C/A;T snv 8.0E-06 0.700 1.000 21 1998 2016
dbSNP: rs185638763
rs185638763
SCN5A
4 0.882 0.120 3 38599001 missense variant G/A;T snv 1.2E-05 0.700 1.000 21 1998 2016
dbSNP: rs193922726
rs193922726
SCN5A
1 1.000 0.080 3 38551188 missense variant G/A;C snv 6.0E-05 0.700 1.000 21 1998 2016
dbSNP: rs199473050
rs199473050
SCN5A
1 1.000 0.080 3 38633098 missense variant A/C snv 4.4E-05 1.4E-05 0.700 1.000 21 1998 2016
dbSNP: rs199473051
rs199473051
SCN5A
2 0.925 0.120 3 38633058 missense variant C/T snv 0.700 1.000 21 1998 2016
dbSNP: rs199473052
rs199473052
SCN5A
1 1.000 0.080 3 38630425 missense variant A/G snv 0.700 1.000 21 1998 2016
dbSNP: rs199473053
rs199473053
SCN5A
1 1.000 0.080 3 38630422 missense variant A/C snv 0.700 1.000 21 1998 2016
dbSNP: rs199473054
rs199473054
SCN5A
1 1.000 0.080 3 38630420 missense variant C/G;T snv 2.0E-05; 2.8E-05 0.700 1.000 21 1998 2016
dbSNP: rs199473055
rs199473055
SCN5A
3 0.882 0.120 3 38630393 missense variant G/A;C snv 4.0E-06 0.700 1.000 21 1998 2016
dbSNP: rs199473056
rs199473056
SCN5A
1 1.000 0.080 3 38630376 missense variant G/A;T snv 3.6E-05; 4.0E-06 0.700 1.000 21 1998 2016
dbSNP: rs199473058
rs199473058
SCN5A
2 0.925 0.080 3 38630341 missense variant C/T snv 4.0E-06 0.700 1.000 21 1998 2016
dbSNP: rs199473062
rs199473062
SCN5A
5 0.827 0.120 3 38622401 stop gained C/A;G;T snv 4.1E-06 0.700 1.000 21 1998 2016