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: rs201698592
rs201698592
KCNQ1 ; KCNQ1-AS1
2 0.925 0.080 11 2847916 synonymous variant C/T snv 1.7E-04 2.8E-05 0.010 1.000 1 2020 2020
dbSNP: rs45546039
rs45546039
SCN5A
15 0.732 0.120 3 38613781 missense variant C/A;T snv 4.1E-06 0.010 1.000 1 2018 2018
dbSNP: rs5443
rs5443
GNB3 ; CDCA3
106 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 0.010 1.000 1 2006 2006
dbSNP: rs56984562
rs56984562
LMNA
6 0.827 0.200 1 156137666 missense variant C/A;G;T snv 0.010 1.000 1 2010 2010
dbSNP: rs59301204
rs59301204
LMNA
4 0.925 0.080 1 156135956 missense variant G/A;C snv 1.2E-05 0.010 1.000 1 2017 2017
dbSNP: rs740952
rs740952
KCNH2
2 0.925 0.080 7 150952515 synonymous variant G/A;T snv 0.30; 7.2E-05 0.010 1.000 1 2020 2020
dbSNP: rs750678689
rs750678689
SCN5A
2 0.925 0.080 3 38566466 synonymous variant G/A snv 8.0E-06 2.1E-05 0.010 1.000 1 2020 2020
dbSNP: rs755373114
rs755373114
ANK2
3 0.925 0.080 4 113341742 missense variant A/C snv 7.2E-05 0.010 1.000 1 2018 2018
dbSNP: rs761056344
rs761056344
PLN ; CEP85L
3 0.925 0.080 6 118558994 missense variant C/G;T snv 4.0E-06; 3.2E-05 0.010 1.000 1 2015 2015
dbSNP: rs764772142
rs764772142
RYR2
2 0.925 0.080 1 237377349 missense variant C/A;T snv 8.0E-06 0.010 1.000 1 2019 2019
dbSNP: rs765835441
rs765835441
RYR2
1 1.000 0.080 1 237726291 missense variant C/T snv 2.7E-05 2.1E-05 0.010 1.000 1 2011 2011
dbSNP: rs794728708
rs794728708
RYR2
8 0.827 0.120 1 237377386 missense variant G/A;T snv 0.010 1.000 1 2009 2009