Gene: MIR3681HG
Alternate names for this Gene: -
Gene Summary:
Gene is located in Chromosome: 2
Location in Chromosome : 2p24.3
Description of this Gene: MIR3681 host gene
Type of Gene: ncRNA
rs1534430 in
MIR3681HG gene and
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1
PMID 30595370 2019 Leveraging Polygenic Functional Enrichment to Improve GWAS Power.
rs1534430 in
MIR3681HG gene and
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2
PMID 30595370 2019 Leveraging Polygenic Functional Enrichment to Improve GWAS Power.
rs1534430 in
MIR3681HG gene and
AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6
PMID 30595370 2019 Leveraging Polygenic Functional Enrichment to Improve GWAS Power.
rs6709385 in
MIR3681HG gene and
Adolescent idiopathic scoliosis
PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.
rs11690527 in
MIR3681HG gene and
Asthma
PMID 22694930 2012 Genome-wide association studies of asthma indicate opposite immunopathogenesis direction from autoimmune diseases.
rs1534430 in
MIR3681HG gene and
Autoimmune Diseases
PMID 30595370 2019 Leveraging Polygenic Functional Enrichment to Improve GWAS Power.
rs1534422 in
MIR3681HG gene and
Autoimmune thyroiditis
PMID 22922229 2012 Seven newly identified loci for autoimmune thyroid disease.
rs13022088 in
MIR3681HG gene and
Body Height
PMID 30595370 2019 Leveraging Polygenic Functional Enrichment to Improve GWAS Power.
rs893787 in
MIR3681HG gene and
Essential Tremor
PMID 27797806 2016 Genome-wide association study in essential tremor identifies three new loci.
rs116375068 in
MIR3681HG gene and
Forced expiratory volume function
PMID 26634245 2015 A genome-wide association study identifies risk loci for spirometric measures among smokers of European and African ancestry.
rs1595810 in
MIR3681HG gene and
Glomerular Filtration Rate
PMID 31152163 2019 A catalog of genetic loci associated with kidney function from analyses of a million individuals.
rs1534422 in
MIR3681HG gene and
Graves Disease
PMID 22922229 2012 Seven newly identified loci for autoimmune thyroid disease.
rs1534422 in
MIR3681HG gene and
Hashimoto Disease
PMID 22922229 2012 Seven newly identified loci for autoimmune thyroid disease.
rs1534430 in
MIR3681HG gene and
Hypothyroidism
PMID 30595370 2019 Leveraging Polygenic Functional Enrichment to Improve GWAS Power.
rs1030893 in
MIR3681HG gene and
Leukemia, Myelocytic, Acute
PMID 27903959 2017 Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia.
rs1534422 in
MIR3681HG gene and
Multiple Sclerosis
PMID 24076602 2013 Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis.
rs62115045 in
MIR3681HG gene and
Plexiform leiomyoma
PMID 31649266 2019 Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis.
rs16858228 in
MIR3681HG gene and
Polysomnography
PMID 23251661 2012 Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population.
rs6709385 in
MIR3681HG gene and
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.
rs62115045 in
MIR3681HG gene and
Uterine Fibroids
PMID 31649266 2019 Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis.
rs62124708 in
MIR3681HG gene and
mathematical ability
PMID 30038396 2018 Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals.