Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2293688
rs2293688
Entrez Id: 55851;199746
Gene Symbol: PSENEN;U2AF1L4
PSENEN;U2AF1L4
CUI: C0596887
Disease:
mathematical ability 		C 0.700 GeneticVariation GWASCAT Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. 30038396 2018
dbSNP: rs1555738837
rs1555738837
Entrez Id: 55851;199746
Gene Symbol: PSENEN;U2AF1L4
PSENEN;U2AF1L4
CUI: C3151037
Disease:
ACNE INVERSA, FAMILIAL, 2, WITH OR WITHOUT DOWLING-DEGOS DISEASE 		A 0.700 CausalMutation CLINVAR
dbSNP: rs1555738906
rs1555738906
Entrez Id: 55851;55957;199746
Gene Symbol: PSENEN;LIN37;U2AF1L4
PSENEN;LIN37;U2AF1L4
CUI: C3151037
Disease:
ACNE INVERSA, FAMILIAL, 2, WITH OR WITHOUT DOWLING-DEGOS DISEASE 		G 0.700 CausalMutation CLINVAR
dbSNP: rs3817622
rs3817622
Entrez Id: 55851;199746
Gene Symbol: PSENEN;U2AF1L4
PSENEN;U2AF1L4
CUI: C0494463
Disease:
Alzheimer Disease, Late Onset 		0.010 GeneticVariation BEFREE Our results suggest that there is an association between rs3817622 and the development of LOAD in APOE epsilon4 carriers within the northern Chinese population. 17280645 2007