Source: BEFREE

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: rs104894021
rs104894021
0.851 0.120 7 150951629 missense variant G/C;T snv
CUI: C2348199
Disease: Short Qt Syndrome
Short Qt Syndrome
0.080 1.000 8 2005 2019
dbSNP: rs199472830
rs199472830
0.925 0.120 7 150974931 missense variant G/T snv
CUI: C0023976
Disease: Long QT Syndrome
Long QT Syndrome
0.030 1.000 3 1999 2015
dbSNP: rs199472936
rs199472936
0.882 0.120 7 150951592 missense variant C/A;T snv
CUI: C3150943
Disease: Long Qt Syndrome 2
Long Qt Syndrome 2
0.830 1.000 3 1995 2017
dbSNP: rs28928905
rs28928905
0.851 0.120 7 150952514 missense variant C/G;T snv
CUI: C0023976
Disease: Long QT Syndrome
Long QT Syndrome
0.730 1.000 3 2001 2013
dbSNP: rs3800779
rs3800779
1.000 0.040 7 150974126 intron variant C/A;T snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.030 1.000 3 2010 2019
dbSNP: rs121912507
rs121912507
0.882 0.120 7 150951511 missense variant C/G;T snv
CUI: C3150943
Disease: Long Qt Syndrome 2
Long Qt Syndrome 2
0.820 1.000 2 1995 2019
dbSNP: rs121912507
rs121912507
0.882 0.120 7 150951511 missense variant C/G;T snv
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation
0.020 1.000 2 2010 2017
dbSNP: rs1805123
rs1805123
0.724 0.280 7 150948446 missense variant T/A;C;G snv 1.3E-05; 0.18; 8.4E-06
CUI: C0003811
Disease: Cardiac Arrhythmia
Cardiac Arrhythmia
0.020 1.000 2 2010 2017
dbSNP: rs1805123
rs1805123
0.724 0.280 7 150948446 missense variant T/A;C;G snv 1.3E-05; 0.18; 8.4E-06
CUI: C0039070
Disease: Syncope
Syncope
0.020 1.000 2 2011 2017
dbSNP: rs1805123
rs1805123
0.724 0.280 7 150948446 missense variant T/A;C;G snv 1.3E-05; 0.18; 8.4E-06
CUI: C0023976
Disease: Long QT Syndrome
Long QT Syndrome
0.020 1.000 2 2008 2010
dbSNP: rs1805123
rs1805123
0.724 0.280 7 150948446 missense variant T/A;C;G snv 1.3E-05; 0.18; 8.4E-06
Ventricular tachycardia, polymorphic
0.020 1.000 2 2016 2017
dbSNP: rs1805123
rs1805123
0.724 0.280 7 150948446 missense variant T/A;C;G snv 1.3E-05; 0.18; 8.4E-06
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.020 1.000 2 2008 2012
dbSNP: rs199472862
rs199472862
1.000 0.120 7 150959673 missense variant A/C;G snv
CUI: C0023976
Disease: Long QT Syndrome
Long QT Syndrome
0.020 1.000 2 2004 2005
dbSNP: rs199472918
rs199472918
0.882 0.120 7 150951738 missense variant A/G snv 7.2E-05 5.6E-05
CUI: C0023976
Disease: Long QT Syndrome
Long QT Syndrome
0.720 1.000 2 2000 2014
dbSNP: rs199472947
rs199472947
1.000 0.080 7 150951540 missense variant G/A;C snv
CUI: C2348199
Disease: Short Qt Syndrome
Short Qt Syndrome
0.020 1.000 2 2011 2019
dbSNP: rs199473024
rs199473024
7 150947362 missense variant T/C snv 7.0E-06
CUI: C0003811
Disease: Cardiac Arrhythmia
Cardiac Arrhythmia
0.020 1.000 2 2014 2018
dbSNP: rs199473529
rs199473529
1.000 0.120 7 150951475 missense variant A/C;G snv
CUI: C3150943
Disease: Long Qt Syndrome 2
Long Qt Syndrome 2
0.720 1.000 2 1995 2009
dbSNP: rs28928904
rs28928904
0.925 0.120 7 150951615 missense variant A/C;G;T snv 4.0E-06
CUI: C0023976
Disease: Long QT Syndrome
Long QT Syndrome
0.720 1.000 2 1996 2005
dbSNP: rs767910122
rs767910122
0.724 0.280 7 150948446 frameshift variant -/GTCCG ins 4.4E-05
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.020 1.000 2 2008 2012
dbSNP: rs767910122
rs767910122
0.724 0.280 7 150948446 frameshift variant -/GTCCG ins 4.4E-05
CUI: C0039070
Disease: Syncope
Syncope
0.020 1.000 2 2011 2017
dbSNP: rs767910122
rs767910122
0.724 0.280 7 150948446 frameshift variant -/GTCCG ins 4.4E-05
Ventricular tachycardia, polymorphic
0.020 1.000 2 2016 2017
dbSNP: rs767910122
rs767910122
0.724 0.280 7 150948446 frameshift variant -/GTCCG ins 4.4E-05
CUI: C0023976
Disease: Long QT Syndrome
Long QT Syndrome
0.020 1.000 2 2008 2010
dbSNP: rs767910122
rs767910122
0.724 0.280 7 150948446 frameshift variant -/GTCCG ins 4.4E-05
CUI: C0003811
Disease: Cardiac Arrhythmia
Cardiac Arrhythmia
0.020 1.000 2 2010 2017
dbSNP: rs769505732
rs769505732
0.925 0.120 7 150952696 missense variant G/A snv 4.0E-06
CUI: C1141890
Disease: Congenital long QT syndrome
Congenital long QT syndrome
0.020 1.000 2 2005 2013
dbSNP: rs794728448
rs794728448
0.724 0.280 7 150948445 frameshift variant CT/G delins
CUI: C0023976
Disease: Long QT Syndrome
Long QT Syndrome
0.020 1.000 2 2008 2010