rs41261344, SCN5A

N. diseases: 11
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Brugada Syndrome 1
CUI: C4551804
Disease: Brugada Syndrome 1
234 0.763 0.120 3 38575385 missense variant C/T snv 5.4E-03 2.2E-03 0.700 0
LONG QT SYNDROME 3
CUI: C1859062
Disease: LONG QT SYNDROME 3
157 0.763 0.120 3 38575385 missense variant C/T snv 5.4E-03 2.2E-03 0.700 0
Long QT Syndrome
CUI: C0023976
Disease: Long QT Syndrome
349 0.763 0.120 3 38575385 missense variant C/T snv 5.4E-03 2.2E-03 0.050 1.000 5 2006 2019
Brugada Syndrome (disorder)
CUI: C1142166
Disease: Brugada Syndrome (disorder)
201 0.763 0.120 3 38575385 missense variant C/T snv 5.4E-03 2.2E-03 0.030 1.000 3 2005 2019
Sudden unexpected nocturnal death syndrome
CUI: C2930805
Disease: Sudden unexpected nocturnal death syndrome
1 0.763 0.120 3 38575385 missense variant C/T snv 5.4E-03 2.2E-03 0.020 1.000 2 2005 2012
Atrial Fibrillation
CUI: C0004238
Disease: Atrial Fibrillation
584 0.763 0.120 3 38575385 missense variant C/T snv 5.4E-03 2.2E-03 0.010 1.000 1 2019 2019
Body Temperature Changes
CUI: C0005904
Disease: Body Temperature Changes
1 0.763 0.120 3 38575385 missense variant C/T snv 5.4E-03 2.2E-03 0.010 1.000 1 2018 2018
Cardiomyopathy, Dilated
CUI: C0007193
Disease: Cardiomyopathy, Dilated
509 0.763 0.120 3 38575385 missense variant C/T snv 5.4E-03 2.2E-03 0.010 1.000 1 2012 2012
Channelopathies
CUI: C1720983
Disease: Channelopathies
8 0.763 0.120 3 38575385 missense variant C/T snv 5.4E-03 2.2E-03 0.010 1.000 1 2012 2012
Familial (FPAH)
CUI: C1611743
Disease: Familial (FPAH)
276 0.763 0.120 3 38575385 missense variant C/T snv 5.4E-03 2.2E-03 0.010 1.000 1 2005 2005
Obstructive sleep apnea hypopnea syndrome
CUI: C4285910
Disease: Obstructive sleep apnea hypopnea syndrome
7 0.763 0.120 3 38575385 missense variant C/T snv 5.4E-03 2.2E-03 0.010 1.000 1 2009 2009