Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs28937318
rs28937318
0.925 0.080 3 38606709 missense variant C/A;T snv
CUI: C1142166
Disease: Brugada Syndrome (disorder)
Brugada Syndrome (disorder)
0.720 1.000 11 2002 2018
dbSNP: rs199473311
rs199473311
0.882 0.120 3 38551070 missense variant T/C snv 7.0E-06
CUI: C1142166
Disease: Brugada Syndrome (disorder)
Brugada Syndrome (disorder)
0.700 1.000 9 2002 2015
dbSNP: rs137854600
rs137854600
0.807 0.120 3 38551504 missense variant C/A;T snv
CUI: C1142166
Disease: Brugada Syndrome (disorder)
Brugada Syndrome (disorder)
0.700 1.000 7 1998 2010
dbSNP: rs199473556
rs199473556
0.851 0.120 3 38630342 missense variant G/A snv
CUI: C1142166
Disease: Brugada Syndrome (disorder)
Brugada Syndrome (disorder)
0.700 1.000 7 2009 2015
dbSNP: rs137854607
rs137854607
0.882 0.120 3 38554309 missense variant C/G;T snv
CUI: C1142166
Disease: Brugada Syndrome (disorder)
Brugada Syndrome (disorder)
0.700 1.000 5 2002 2012
dbSNP: rs1553705586
rs1553705586
1.000 0.080 3 38609966 splice acceptor variant T/C snv
CUI: C1142166
Disease: Brugada Syndrome (disorder)
Brugada Syndrome (disorder)
0.700 1.000 5 1998 2012
dbSNP: rs199473161
rs199473161
1.000 0.080 3 38586038 missense variant G/A;T snv
CUI: C1142166
Disease: Brugada Syndrome (disorder)
Brugada Syndrome (disorder)
0.700 1.000 5 2005 2015
dbSNP: rs199473305
rs199473305
0.925 0.080 3 38551145 missense variant C/T snv 1.4E-05
CUI: C1142166
Disease: Brugada Syndrome (disorder)
Brugada Syndrome (disorder)
0.700 1.000 5 2003 2015
dbSNP: rs727504801
rs727504801
0.925 0.080 3 38560397 frameshift variant G/- delins
CUI: C1142166
Disease: Brugada Syndrome (disorder)
Brugada Syndrome (disorder)
0.700 1.000 5 1998 2012
dbSNP: rs137854614
rs137854614
0.882 0.120 3 38550988 missense variant T/C snv
CUI: C1142166
Disease: Brugada Syndrome (disorder)
Brugada Syndrome (disorder)
0.720 1.000 4 2001 2008
dbSNP: rs397514450
rs397514450
0.925 0.080 3 38585926 frameshift variant -/AC delins
CUI: C1142166
Disease: Brugada Syndrome (disorder)
Brugada Syndrome (disorder)
0.700 1.000 4 2005 2017
dbSNP: rs794728849
rs794728849
0.925 0.120 3 38613782 stop gained G/A;C snv
CUI: C1142166
Disease: Brugada Syndrome (disorder)
Brugada Syndrome (disorder)
0.710 1.000 4 2009 2016
dbSNP: rs794728914
rs794728914
1.000 0.080 3 38585895 frameshift variant AA/- delins
CUI: C1142166
Disease: Brugada Syndrome (disorder)
Brugada Syndrome (disorder)
0.700 1.000 4 2003 2012
dbSNP: rs878855296
rs878855296
0.925 0.080 3 38613790 missense variant C/T snv 7.0E-06
CUI: C1142166
Disease: Brugada Syndrome (disorder)
Brugada Syndrome (disorder)
0.700 1.000 4 2012 2015
dbSNP: rs72549410
rs72549410
0.851 0.120 3 38606058 missense variant C/T snv
CUI: C1142166
Disease: Brugada Syndrome (disorder)
Brugada Syndrome (disorder)
0.700 1.000 3 2000 2015
dbSNP: rs727505158
rs727505158
0.925 0.080 3 38599005 frameshift variant G/- delins 1.4E-05
CUI: C1142166
Disease: Brugada Syndrome (disorder)
Brugada Syndrome (disorder)
0.700 1.000 3 2010 2012
dbSNP: rs794728843
rs794728843
0.925 0.080 3 38620842 splice donor variant C/T snv 7.0E-06
CUI: C1142166
Disease: Brugada Syndrome (disorder)
Brugada Syndrome (disorder)
0.700 1.000 3 2010 2014
dbSNP: rs863225273
rs863225273
1.000 0.080 3 38554320 stop gained C/T snv
CUI: C1142166
Disease: Brugada Syndrome (disorder)
Brugada Syndrome (disorder)
0.700 1.000 3 2004 2010
dbSNP: rs869025522
rs869025522
1.000 0.080 3 38555719 inframe deletion TCT/- delins 7.0E-06
CUI: C1142166
Disease: Brugada Syndrome (disorder)
Brugada Syndrome (disorder)
0.700 1.000 3 2009 2013
dbSNP: rs1060501135
rs1060501135
1.000 0.080 3 38581226 stop gained C/T snv
CUI: C1142166
Disease: Brugada Syndrome (disorder)
Brugada Syndrome (disorder)
0.700 1.000 2 2010 2012
dbSNP: rs1553692660
rs1553692660
1.000 0.080 3 38550910 frameshift variant AG/- del
CUI: C1142166
Disease: Brugada Syndrome (disorder)
Brugada Syndrome (disorder)
0.700 1.000 2 2009 2017
dbSNP: rs1553700699
rs1553700699
1.000 0.080 3 38586012 stop gained C/T snv
CUI: C1142166
Disease: Brugada Syndrome (disorder)
Brugada Syndrome (disorder)
0.700 1.000 2 2005 2008
dbSNP: rs786204839
rs786204839
1.000 0.080 3 38605949 splice donor variant A/G;T snv
CUI: C1142166
Disease: Brugada Syndrome (disorder)
Brugada Syndrome (disorder)
0.700 1.000 2 2010 2012
dbSNP: rs794728865
rs794728865
0.925 0.120 3 38585903 stop gained G/A snv
CUI: C1142166
Disease: Brugada Syndrome (disorder)
Brugada Syndrome (disorder)
0.700 1.000 2 2010 2012
dbSNP: rs869025520
rs869025520
1.000 0.080 3 38579372 stop gained G/A snv
CUI: C1142166
Disease: Brugada Syndrome (disorder)
Brugada Syndrome (disorder)
0.700 1.000 2 2002 2013