rs730882262, 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.
Right ventricular cardiomyopathy
CUI: C2063326
Disease: Right ventricular cardiomyopathy
4 0.851 0.160 1 156135293 missense variant T/C;G snv 0.710 1.000 1 2015 2015
Cardiomyopathy, Familial Idiopathic
CUI: C1449563
Disease: Cardiomyopathy, Familial Idiopathic
243 0.851 0.160 1 156135293 missense variant T/C;G snv 0.700 0
Progeria Syndrome, Childhood-Onset
CUI: C2750285
Disease: Progeria Syndrome, Childhood-Onset
3 0.851 0.160 1 156135293 missense variant T/C;G snv 0.700 0
Premature aging syndrome
CUI: C0231341
Disease: Premature aging syndrome
5 0.851 0.160 1 156135293 missense variant T/C;G snv 0.010 1.000 1 2015 2015