SNX27, sorting nexin 27, 81609

N. diseases: 24; N. variants: 2
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1553266166
rs1553266166
Entrez Id: 81609
Gene Symbol: SNX27
SNX27
CUI: C4551549
Disease:
Early Infantile Epileptic Encephalopathy 6 		TA 0.700 CausalMutation CLINVAR
dbSNP: rs201966711
rs201966711
Entrez Id: 81609
Gene Symbol: SNX27
SNX27
CUI: C4551549
Disease:
Early Infantile Epileptic Encephalopathy 6 		G 0.700 CausalMutation CLINVAR