rs267607555, LMNA

N. diseases: 4
Source: INFERRED ×
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.
Familial Partial Lipodystrophy, Type 2
CUI: C1720860
Disease: Familial Partial Lipodystrophy, Type 2
0.807 0.280 1 156136009 missense variant C/T snv 7.0E-06 0.710 1.000 0 2020 2020
Hereditary Motor and Sensory-Neuropathy Type II
CUI: C0270914
Disease: Hereditary Motor and Sensory-Neuropathy Type II
0.807 0.280 1 156136009 missense variant C/T snv 7.0E-06 0.700 1.000 9 2004 2017
Hyperglycemia
CUI: C0020456
Disease: Hyperglycemia
0.807 0.280 1 156136009 missense variant C/T snv 7.0E-06 0.700 1.000 5 1990 2013
Monogenic diabetes
CUI: C3888631
Disease: Monogenic diabetes
0.807 0.280 1 156136009 missense variant C/T snv 7.0E-06 0.700 1.000 5 1990 2013