MYL4, myosin light chain 4, 4635

N. diseases: 26; N. variants: 5
Disease: familial atrial fibrillation ×
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: rs886037778
rs886037778 		1.000 17 47209453 missense variant G/A snv
CUI: C3468561
Disease: familial atrial fibrillation
familial atrial fibrillation 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.700 1.000 1 2016 2016