rs61672878, LMNA

N. diseases: 11
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.
Autosomal Dominant Emery-Dreifuss Muscular Dystrophy (disorder)
74 0.776 0.200 1 156136094 missense variant G/A;T snv 0.710 1.000 1 2004 2004
Hereditary Motor and Sensory-Neuropathy Type II
144 0.776 0.200 1 156136094 missense variant G/A;T snv 0.700 1.000 11 2000 2016
Muscular Dystrophy
CUI: C0026850
Disease: Muscular Dystrophy
67 0.776 0.200 1 156136094 missense variant G/A;T snv 0.700 0
Cardiomyopathy, Familial Idiopathic
CUI: C1449563
Disease: Cardiomyopathy, Familial Idiopathic
243 0.776 0.200 1 156136094 missense variant G/A;T snv 0.020 1.000 2 2003 2003
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1B (disorder)
6 0.776 0.200 1 156136094 missense variant G/A;T snv 0.020 0.500 2 2002 2016
Myopathy
CUI: C0026848
Disease: Myopathy
166 0.776 0.200 1 156136094 missense variant G/A;T snv 0.020 1.000 2 2003 2016
Atrial Fibrillation
CUI: C0004238
Disease: Atrial Fibrillation
584 0.776 0.200 1 156136094 missense variant G/A;T snv 0.010 1.000 1 2003 2003
Muscle Weakness
CUI: C0151786
Disease: Muscle Weakness
87 0.776 0.200 1 156136094 missense variant G/A;T snv 0.010 1.000 1 2016 2016
Muscular Dystrophy, Emery-Dreifuss
CUI: C0410189
Disease: Muscular Dystrophy, Emery-Dreifuss
18 0.776 0.200 1 156136094 missense variant G/A;T snv 0.010 1.000 1 2004 2004
Paresis
CUI: C0030552
Disease: Paresis
49 0.776 0.200 1 156136094 missense variant G/A;T snv 0.010 1.000 1 2016 2016
Polyneuropathy
CUI: C0152025
Disease: Polyneuropathy
32 0.776 0.200 1 156136094 missense variant G/A;T snv 0.010 1.000 1 2015 2015