LMO7, LIM domain 7, 4008

N. diseases: 25; N. variants: 14
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: rs4884021
rs4884021
1.000 0.040 13 75823595 missense variant G/A snv 0.18 0.24
CUI: C1449563
Disease: Cardiomyopathy, Familial Idiopathic
Cardiomyopathy, Familial Idiopathic
Cardiovascular Diseases 0.010 1.000 1 2017 2017
dbSNP: rs7986131
rs7986131
1.000 0.040 13 75849112 missense variant T/C snv 0.72 0.71
CUI: C1449563
Disease: Cardiomyopathy, Familial Idiopathic
Cardiomyopathy, Familial Idiopathic
Cardiovascular Diseases 0.010 1.000 1 2017 2017