Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1250554906
rs1250554906
TNF
CUI: C0393814
Disease: Hereditary liability to pressure palsies
Hereditary liability to pressure palsies 		0.010 GeneticVariation BEFREE In our patients, early-onset HNPP was associated frequently with isoleucine92valine LITAF polymorphism. 24668782

2014