ERLIN2, ER lipid raft associated 2, 11160

N. diseases: 85; N. variants: 4
Disease: Spastic Paraplegia, Hereditary ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs763958615
rs763958615
Entrez Id: 11160
Gene Symbol: ERLIN2
ERLIN2
CUI: C0037773
Disease:
Spastic Paraplegia, Hereditary 		T 0.700 GeneticVariation CLINVAR Massive sequencing of 70 genes reveals a myriad of missing genes or mechanisms to be uncovered in hereditary spastic paraplegias. 28832565 2017