Gene: IFITM2
Alternate names for this Gene:
1-8D|DSPA2c
Gene Summary:
Gene is located in Chromosome:
11
Location in Chromosome :
11p15.5
Description of this Gene:
interferon induced transmembrane protein 2
Type of Gene:
protein-coding
rs14408
in
IFITM2
gene and
Blood basophil count (lab test)
PMID 27863252
2016 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.
rs1059091
in
IFITM2
gene and
Eosinophil count procedure
PMID 30595370
2019 Leveraging Polygenic Functional Enrichment to Improve GWAS Power.
PMID 27863252
2016 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.
rs14408
in
IFITM2
gene and
Granulocyte count
PMID 27863252
2016 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.
rs10751647
in
IFITM2
gene and
Monocyte count procedure
PMID 27863252
2016 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.
rs10751647
in
IFITM2
gene and
Monocyte count result
PMID 27863252
2016 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.
rs14408
in
IFITM2
gene and
Neutrophil count (procedure)
PMID 27863252
2016 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.
rs9704108
in
IFITM2
gene and
Platelet Count measurement
PMID 27863252
2016 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.
rs1058900
in
IFITM2
gene and
Red Blood Cell Count measurement
PMID 30595370
2019 Leveraging Polygenic Functional Enrichment to Improve GWAS Power.
rs28521954
in
IFITM2
gene and
White Blood Cell Count procedure
PMID 27863252
2016 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.
PMID 30595370
2019 Leveraging Polygenic Functional Enrichment to Improve GWAS Power.