rs104894485, HCN4

N. diseases: 4
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.
Sick Sinus Syndrome 2, Autosomal Dominant
CUI: C1834144
Disease: Sick Sinus Syndrome 2, Autosomal Dominant
5 0.882 0.080 15 73325378 missense variant C/T snv 3.6E-05 7.0E-06 0.800 1.000 4 2004 2012
Sinus Node Dysfunction (disorder)
CUI: C0428908
Disease: Sinus Node Dysfunction (disorder)
7 0.882 0.080 15 73325378 missense variant C/T snv 3.6E-05 7.0E-06 0.010 1.000 1 2004 2004
Syncope
CUI: C0039070
Disease: Syncope
45 0.882 0.080 15 73325378 missense variant C/T snv 3.6E-05 7.0E-06 0.010 1.000 1 2004 2004
Ventricular tachycardia, polymorphic
CUI: C0344432
Disease: Ventricular tachycardia, polymorphic
11 0.882 0.080 15 73325378 missense variant C/T snv 3.6E-05 7.0E-06 0.010 1.000 1 2004 2004