CLCN6, chloride voltage-gated channel 6, 1185

N. diseases: 24; N. variants: 25
Disease: Atrial Fibrillation, Familial, 6 ×
Source: ALL
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: rs587776851
rs587776851 		1.000 0.080 1 11846008 stop lost TT/- del
CUI: C2677294
Disease: Atrial Fibrillation, Familial, 6
Atrial Fibrillation, Familial, 6 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.700 0
dbSNP: rs61757261
rs61757261 		0.925 0.080 1 11847373 missense variant T/G snv 2.0E-03 1.6E-03
CUI: C2677294
Disease: Atrial Fibrillation, Familial, 6
Atrial Fibrillation, Familial, 6 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.700 0