rs797044485, LMNA

N. diseases: 4
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Progeria
CUI: C0033300
Disease: Progeria
41 0.851 0.160 1 156134832 missense variant G/A snv 0.700 1.000 1 2013 2013
Arteriosclerosis
CUI: C0003850
Disease: Arteriosclerosis
267 0.851 0.160 1 156134832 missense variant G/A snv 0.010 1.000 1 2013 2013
Atherosclerosis
CUI: C0004153
Disease: Atherosclerosis
281 0.851 0.160 1 156134832 missense variant G/A snv 0.010 1.000 1 2013 2013
Steatohepatitis
CUI: C2711227
Disease: Steatohepatitis
75 0.851 0.160 1 156134832 missense variant G/A snv 0.010 1.000 1 2013 2013