Source: CLINVAR

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: rs137854618
rs137854618
0.734 0.107 3 38566426 missense variant C/A,T snp 8.0E-06
CUI: C1142166
Disease: Brugada Syndrome (disorder)
Brugada Syndrome (disorder)
0.800 11 2003 2017
dbSNP: rs137854618
rs137854618
0.734 0.107 3 38566426 missense variant C/A,T snp 8.0E-06
CUI: C1832680
Disease: CARDIOMYOPATHY, DILATED, 1E
CARDIOMYOPATHY, DILATED, 1E
0.800 5 1986 2006
dbSNP: rs137854618
rs137854618
0.734 0.107 3 38566426 missense variant C/A,T snp 8.0E-06
CUI: C4016652
Disease: ATRIAL STANDSTILL 1, DIGENIC
ATRIAL STANDSTILL 1, DIGENIC
0.700 5 1986 2006
dbSNP: rs137854618
rs137854618
0.734 0.107 3 38566426 missense variant C/A,T snp 8.0E-06
CUI: C3151464
Disease: ATRIAL FIBRILLATION, FAMILIAL, 10
ATRIAL FIBRILLATION, FAMILIAL, 10
0.700 5 1986 2006
dbSNP: rs137854618
rs137854618
0.734 0.107 3 38566426 missense variant C/A,T snp 8.0E-06
CUI: C1859062
Disease: LONG QT SYNDROME 3
LONG QT SYNDROME 3
0.700 1 2015 2015