rs121434386, SCN4B

N. diseases: 2
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.
Long Qt Syndrome 10
CUI: C2678484
Disease: Long Qt Syndrome 10
3 0.925 0.120 11 118141265 missense variant G/A snv 7.0E-06 0.800 1.000 1 2007 2007
Congenital long QT syndrome
CUI: C1141890
Disease: Congenital long QT syndrome
54 0.925 0.120 11 118141265 missense variant G/A snv 7.0E-06 0.010 1.000 1 2007 2007