NINJ2, ninjurin 2, 4815

N. diseases: 20; N. variants: 6
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2535393
rs2535393
Entrez Id: 4815
Gene Symbol: NINJ2
NINJ2
CUI: C0023508
Disease:
White Blood Cell Count procedure
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs34038797
rs34038797
Entrez Id: 4815;100049716
Gene Symbol: NINJ2;NINJ2-AS1
NINJ2;NINJ2-AS1
CUI: C0032181
Disease:
Platelet Count measurement
0.700 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010 2018
dbSNP: rs34038797
rs34038797
Entrez Id: 4815;100049716
Gene Symbol: NINJ2;NINJ2-AS1
NINJ2;NINJ2-AS1
CUI: C0032181
Disease:
Platelet Count measurement
G 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs34038797
rs34038797
Entrez Id: 4815;100049716
Gene Symbol: NINJ2;NINJ2-AS1
NINJ2;NINJ2-AS1
CUI: C0200635
Disease:
Lymphocyte Count measurement
G 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs61916664
rs61916664
Entrez Id: 4815
Gene Symbol: NINJ2
NINJ2
CUI: C3828530
Disease:
Platelet Component Distribution Width Measurement
G 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs7487827
rs7487827
Entrez Id: 4815;100049716
Gene Symbol: NINJ2;NINJ2-AS1
NINJ2;NINJ2-AS1
CUI: C0750880
Disease:
Monocyte count result
T 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs7487827
rs7487827
Entrez Id: 4815;100049716
Gene Symbol: NINJ2;NINJ2-AS1
NINJ2;NINJ2-AS1
CUI: C0200637
Disease:
Monocyte count procedure
T 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs3809263
rs3809263
Entrez Id: 4815
Gene Symbol: NINJ2
NINJ2
CUI: C0038454
Disease:
Cerebrovascular accident
0.020 GeneticVariation BEFREE The rs3809263 was associated with risk of s</span>troke in dominant model (OR (95% CI) = 1.5 (1.09-2.06), adjusted P value = 0.02). 31372770 2019
dbSNP: rs3809263
rs3809263
Entrez Id: 4815
Gene Symbol: NINJ2
NINJ2
CUI: C0038454
Disease:
Cerebrovascular accident
0.020 GeneticVariation BEFREE Further validation of the functionality of the NINJ2 rs3809263 G > A polymorphism and its association with risk of LAA stroke in other ethnic populations is warranted. 26687183 2016
dbSNP: rs3809263
rs3809263
Entrez Id: 4815
Gene Symbol: NINJ2
NINJ2
CUI: C0026769
Disease:
Multiple Sclerosis
0.010 GeneticVariation BEFREE Moreover, the rs3809263 was associated with MS risk in recessive model (OR (95% CI) = 2.09 (1.33-3.31), adjusted P value = 0.003). 31292852 2019
dbSNP: rs10849373
rs10849373
Entrez Id: 4815;100049716
Gene Symbol: NINJ2;NINJ2-AS1
NINJ2;NINJ2-AS1
CUI: C0948008
Disease:
Ischemic stroke
0.010 GeneticVariation BEFREE Therefore, we report a new genetic variant, rs10849373, located in the first intron of the NINJ2 gene, conferring risk of ischemic stroke in Chinese Han subjects. 21722921 2011