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
0.742 0.120 3 38566426 missense variant C/A;T snv 8.0E-06
CUI: C3151464
Disease: ATRIAL FIBRILLATION, FAMILIAL, 10
ATRIAL FIBRILLATION, FAMILIAL, 10
0.700 0
dbSNP: rs137854618
rs137854618
0.742 0.120 3 38566426 missense variant C/A;T snv 8.0E-06
CUI: C1859062
Disease: LONG QT SYNDROME 3
LONG QT SYNDROME 3
0.700 0
dbSNP: rs137854618
rs137854618
0.742 0.120 3 38566426 missense variant C/A;T snv 8.0E-06
CUI: C4016652
Disease: ATRIAL STANDSTILL 1, DIGENIC
ATRIAL STANDSTILL 1, DIGENIC
0.700 0
dbSNP: rs137854618
rs137854618
0.742 0.120 3 38566426 missense variant C/A;T snv 8.0E-06
CUI: C1142166
Disease: Brugada Syndrome (disorder)
Brugada Syndrome (disorder)
0.700 1.000 8 2003 2015
dbSNP: rs137854618
rs137854618
0.742 0.120 3 38566426 missense variant C/A;T snv 8.0E-06
CUI: C1832680
Disease: CARDIOMYOPATHY, DILATED, 1E
CARDIOMYOPATHY, DILATED, 1E
0.800 1.000 0 2004 2013