rs7626962, SCN5A

N. diseases: 3
Source: CLINVAR ×
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.
Sudden infant death syndrome
CUI: C0038644
Disease: Sudden infant death syndrome
5 0.790 0.080 3 38579416 missense variant G/A;T snv 1.6E-05; 5.9E-03 0.750 0.800 0 2006 2011
Left ventricular noncompaction
CUI: C1960469
Disease: Left ventricular noncompaction
19 0.790 0.080 3 38579416 missense variant G/A;T snv 1.6E-05; 5.9E-03 0.700 0
LONG QT SYNDROME 3, ACQUIRED, SUSCEPTIBILITY TO (finding)
CUI: C1838527
Disease: LONG QT SYNDROME 3, ACQUIRED, SUSCEPTIBILITY TO (finding)
1 0.790 0.080 3 38579416 missense variant G/A;T snv 1.6E-05; 5.9E-03 0.700 0