LMNA, lamin A/C, 4000

N. diseases: 824; N. variants: 285
Disease: Heart failure ×
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: rs57045855
rs57045855 		0.882 0.040 1 156134464 missense variant A/G;T snv
CUI: C0018801
Disease: Heart failure
Heart failure 		Cardiovascular Diseases 0.010 1.000 1 2006 2006
dbSNP: rs61195471
rs61195471 		0.827 0.160 1 156134496 missense variant G/A snv
CUI: C0018801
Disease: Heart failure
Heart failure 		Cardiovascular Diseases 0.010 1.000 1 2001 2001
dbSNP: rs61661343
rs61661343 		0.851 0.040 1 156130687 missense variant T/C snv
CUI: C0018801
Disease: Heart failure
Heart failure 		Cardiovascular Diseases 0.010 1.000 1 2004 2004