LNX2, ligand of numb-protein X 2, 222484

N. diseases: 5; N. variants: 4
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs76900683
rs76900683
Entrez Id: 222484
Gene Symbol: LNX2
LNX2
CUI: C3828530
Disease:
Platelet Component Distribution Width Measurement 		C 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs76900683
rs76900683
Entrez Id: 222484
Gene Symbol: LNX2
LNX2
CUI: C0200665
Disease:
Platelet mean volume determination (procedure) 		C 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs1014369151
rs1014369151
Entrez Id: 51082;222484
Gene Symbol: POLR1D;LNX2
POLR1D;LNX2
CUI: C3150983
Disease:
TREACHER COLLINS SYNDROME 2 		0.700 GeneticVariation UNIPROT
dbSNP: rs587777841
rs587777841
Entrez Id: 51082;222484
Gene Symbol: POLR1D;LNX2
POLR1D;LNX2
CUI: C3150983
Disease:
TREACHER COLLINS SYNDROME 2 		G 0.700 CausalMutation CLINVAR
dbSNP: rs767196650
rs767196650
Entrez Id: 51082;222484
Gene Symbol: POLR1D;LNX2
POLR1D;LNX2
CUI: C3150983
Disease:
TREACHER COLLINS SYNDROME 2 		0.700 GeneticVariation UNIPROT