Gene: LINC01149
Alternate names for this Gene:
Gene Summary:
Gene is located in Chromosome:
Location in Chromosome :
Description of this Gene:
Type of Gene:
rs7772549
in
LINC01149
gene and
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
PMID 20041166
2009 Common genetic variation and the control of HIV-1 in humans.
rs7772549
in
LINC01149
gene and
AIDS, PROGRESSION TO
PMID 20041166
2009 Common genetic variation and the control of HIV-1 in humans.
rs2395004
in
LINC01149
gene and
Allergic Reaction
PMID 23817569
2013 A genome-wide association meta-analysis of self-reported allergy identifies shared and allergy-specific susceptibility loci.
rs2596464
in
LINC01149
gene and
Ankylosing spondylitis
PMID 22138694
2011 A genome-wide association study in Han Chinese identifies new susceptibility loci for ankylosing spondylitis.
rs2596464
in
LINC01149
gene and
Asthma
PMID 29273806
2018 Multiancestry association study identifies new asthma risk loci that colocalize with immune-cell enhancer marks.
rs2524277
in
LINC01149
gene and
Blood Protein Measurement
PMID 29875488
2018 Genomic atlas of the human plasma proteome.
rs2596464
in
LINC01149
gene and
Childhood asthma
PMID 29273806
2018 Multiancestry association study identifies new asthma risk loci that colocalize with immune-cell enhancer marks.
rs7772549
in
LINC01149
gene and
HIV-1, RESISTANCE TO
PMID 20041166
2009 Common genetic variation and the control of HIV-1 in humans.
rs7772549
in
LINC01149
gene and
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
PMID 20041166
2009 Common genetic variation and the control of HIV-1 in humans.
rs3093958
in
LINC01149
gene and
Intelligence
PMID 29844566
2018 Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function.
rs34624527
in
LINC01149
gene and
Platelet mean volume determination (procedure)
PMID 27863252
2016 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.
rs2523696
in
LINC01149
gene and
RDW - Red blood cell distribution width result
PMID 27863252
2016 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.
rs2523696
in
LINC01149
gene and
Red cell distribution width determination
PMID 27863252
2016 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.
rs3093958
in
LINC01149
gene and
Sarcoidosis
PMID 22952805
2012 Genome-wide association study of African and European Americans implicates multiple shared and ethnic specific loci in sarcoidosis susceptibility.
rs114618162
in
LINC01149
gene and
Schizophrenia
PMID 30285260
2019 Genome-Wide Association Study Detected Novel Susceptibility Genes for Schizophrenia and Shared Trans-Populations/Diseases Genetic Effect.
rs9469003
in
LINC01149
gene and
Stevens-Johnson Syndrome
PMID 21801394
2011 Genome-wide association study of Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis in Europe.
rs9469003
in
LINC01149
gene and
Toxic Epidermal Necrolysis
PMID 21801394
2011 Genome-wide association study of Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis in Europe.
rs12206131
in
LINC01149
gene and
Vitiligo
PMID 20526339
2010 Genome-wide association study for vitiligo identifies susceptibility loci at 6q27 and the MHC.