rs2535393
×
Entrez Id:
4815
Gene Symbol:
NINJ2
NINJ2
White Blood Cell Count procedure
0.700
GeneticVariation
GWASCAT
Leveraging Polygenic Functional Enrichment to Improve GWAS Power.
30595370
2019
rs34038797
NINJ2;NINJ2-AS1
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
rs34038797
NINJ2;NINJ2-AS1
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
rs34038797
NINJ2;NINJ2-AS1
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
rs61916664
×
Entrez Id:
4815
Gene Symbol:
NINJ2
NINJ2
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
rs7487827
NINJ2;NINJ2-AS1
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
rs7487827
NINJ2;NINJ2-AS1
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
rs3809263
×
Entrez Id:
4815
Gene Symbol:
NINJ2
NINJ2
Cerebrovascular accident
0.020
GeneticVariation
BEFREE
The rs3809263 was associated with risk of s</span>troke in dominant model (OR (9 5% CI) = 1.5 (1.09-2.06), adjusted P value = 0.02).
31372770
2019
rs3809263
×
Entrez Id:
4815
Gene Symbol:
NINJ2
NINJ2
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
rs3809263
×
Entrez Id:
4815
Gene Symbol:
NINJ2
NINJ2
Multiple Sclerosis
0.010
GeneticVariation
BEFREE
Moreover, the rs3809263 was associated wit h MS risk in recessive model (O R (95% CI) = 2.09 (1.33-3.31), adjusted P value = 0.003).
31292852
2019
rs10849373
NINJ2;NINJ2-AS1
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