Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1800629
rs1800629
TNF
CUI: C4749367
Disease: Mesial temporal lobe epilepsy with hippocampal sclerosis
Mesial temporal lobe epilepsy with hippocampal sclerosis 		0.010 GeneticVariation BEFREE No association was observed between rs1800629 genotypes or HLA-DRB1 alleles and MTLE-HS susceptibility. 28675059

2018