rs267607619, LMNA

N. diseases: 3
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.
Atypical Werner syndrome
CUI: C4275075
Disease: Atypical Werner syndrome
4 0.882 0.160 1 156130666 missense variant G/C snv 0.010 1.000 1 2015 2015
Familial generalized lipodystrophy
CUI: C0221032
Disease: Familial generalized lipodystrophy
15 0.882 0.160 1 156130666 missense variant G/C snv 0.010 1.000 1 2015 2015
Generalized Lipodystrophy
CUI: C4317112
Disease: Generalized Lipodystrophy
5 0.882 0.160 1 156130666 missense variant G/C snv 0.010 1.000 1 2015 2015