Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs6790396
rs6790396
1.000 0.080 3 38730434 intron variant C/G snv 0.67
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.700 1.000 2 2018 2018
dbSNP: rs6795970
rs6795970
0.807 0.200 3 38725184 missense variant A/G snv 0.65 0.70
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.020 1.000 2 2014 2017
dbSNP: rs6800541
rs6800541
1.000 0.080 3 38733341 intron variant C/T snv 0.70
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.020 1.000 2 2015 2017
dbSNP: rs10428132
rs10428132
0.925 0.120 3 38736063 intron variant T/G snv 0.67
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.010 1.000 1 2014 2014
dbSNP: rs12632942
rs12632942
1.000 0.080 3 38723507 missense variant A/G snv 0.24 0.22
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.010 1.000 1 2014 2014
dbSNP: rs6771157
rs6771157
1.000 0.080 3 38722372 synonymous variant G/C snv 0.24 0.22
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.010 1.000 1 2016 2016