MIR3681HG, MIR3681 host gene, 100506457

N. diseases: 21; N. variants: 18
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs13022088
rs13022088
Entrez Id: 100506457
Gene Symbol: MIR3681HG
MIR3681HG
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs1534430
rs1534430
Entrez Id: 100506457
Gene Symbol: MIR3681HG
MIR3681HG
CUI: C3150797
Disease:
AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs1534430
rs1534430
Entrez Id: 100506457
Gene Symbol: MIR3681HG
MIR3681HG
CUI: C4014795
Disease:
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs1534430
rs1534430
Entrez Id: 100506457
Gene Symbol: MIR3681HG
MIR3681HG
CUI: C4310768
Disease:
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs1534430
rs1534430
Entrez Id: 100506457
Gene Symbol: MIR3681HG
MIR3681HG
CUI: C0020676
Disease:
Hypothyroidism 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs1534430
rs1534430
Entrez Id: 100506457
Gene Symbol: MIR3681HG
MIR3681HG
CUI: C0004364
Disease:
Autoimmune Diseases 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs1595810
rs1595810
Entrez Id: 100506457
Gene Symbol: MIR3681HG
MIR3681HG
CUI: C0017654
Disease:
Glomerular Filtration Rate 		A 0.700 GeneticVariation GWASCAT A catalog of genetic loci associated with kidney function from analyses of a million individuals. 31152163 2019
dbSNP: rs62115045
rs62115045
Entrez Id: 100506457
Gene Symbol: MIR3681HG
MIR3681HG
CUI: C2242776
Disease:
Plexiform leiomyoma 		A 0.700 GeneticVariation GWASCAT Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis. 31649266 2019
dbSNP: rs62115045
rs62115045
Entrez Id: 100506457
Gene Symbol: MIR3681HG
MIR3681HG
CUI: C0042133
Disease:
Uterine Fibroids 		A 0.700 GeneticVariation GWASCAT Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis. 31649266 2019
dbSNP: rs6432244
rs6432244
Entrez Id: 100506457
Gene Symbol: MIR3681HG
MIR3681HG
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs62124708
rs62124708
Entrez Id: 100506457
Gene Symbol: MIR3681HG
MIR3681HG
CUI: C0596887
Disease:
mathematical ability 		T 0.700 GeneticVariation GWASCAT Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. 30038396 2018
dbSNP: rs62124717
rs62124717
Entrez Id: 100506457
Gene Symbol: MIR3681HG
MIR3681HG
CUI: C0596887
Disease:
mathematical ability 		A 0.700 GeneticVariation GWASCAT Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. 30038396 2018
dbSNP: rs6709385
rs6709385
Entrez Id: 100506457
Gene Symbol: MIR3681HG
MIR3681HG
CUI: C0410702
Disease:
Adolescent idiopathic scoliosis 		0.700 GeneticVariation GWASCAT 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. 30019117 2018
dbSNP: rs6709385
rs6709385
Entrez Id: 100506457
Gene Symbol: MIR3681HG
MIR3681HG
CUI: C1837461
Disease:
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 GeneticVariation GWASCAT 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. 30019117 2018
dbSNP: rs1030893
rs1030893
Entrez Id: 100506457
Gene Symbol: MIR3681HG
MIR3681HG
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		G 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs11894033
rs11894033
Entrez Id: 100506457
Gene Symbol: MIR3681HG
MIR3681HG
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		A 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs17605562
rs17605562
Entrez Id: 100506457
Gene Symbol: MIR3681HG
MIR3681HG
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		C 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs893341
rs893341
Entrez Id: 100506457
Gene Symbol: MIR3681HG
MIR3681HG
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		T 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs893787
rs893787
Entrez Id: 100506457
Gene Symbol: MIR3681HG
MIR3681HG
CUI: C0270736
Disease:
Essential Tremor 		C 0.700 GeneticVariation GWASCAT Genome-wide association study in essential tremor identifies three new loci. 27797806 2016
dbSNP: rs116375068
rs116375068
Entrez Id: 100506457
Gene Symbol: MIR3681HG
MIR3681HG
CUI: C0016529
Disease:
Forced expiratory volume function 		A 0.700 GeneticVariation GWASCAT A genome-wide association study identifies risk loci for spirometric measures among smokers of European and African ancestry. 26634245 2015
dbSNP: rs1534422
rs1534422
Entrez Id: 100506457
Gene Symbol: MIR3681HG
MIR3681HG
CUI: C0026769
Disease:
Multiple Sclerosis 		G 0.700 GeneticVariation GWASCAT Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis. 24076602 2013
dbSNP: rs11690527
rs11690527
Entrez Id: 100506457
Gene Symbol: MIR3681HG
MIR3681HG
CUI: C0004096
Disease:
Asthma 		0.700 GeneticVariation GWASDB Genome-wide association studies of asthma indicate opposite immunopathogenesis direction from autoimmune diseases. 22694930 2012
dbSNP: rs1534422
rs1534422
Entrez Id: 100506457
Gene Symbol: MIR3681HG
MIR3681HG
CUI: C0677607
Disease:
Hashimoto Disease 		G 0.700 GeneticVariation GWASCAT Seven newly identified loci for autoimmune thyroid disease. 22922229 2012
dbSNP: rs1534422
rs1534422
Entrez Id: 100506457
Gene Symbol: MIR3681HG
MIR3681HG
CUI: C0018213
Disease:
Graves Disease 		G 0.700 GeneticVariation GWASCAT Seven newly identified loci for autoimmune thyroid disease. 22922229 2012
dbSNP: rs1534422
rs1534422
Entrez Id: 100506457
Gene Symbol: MIR3681HG
MIR3681HG
CUI: C0920350
Disease:
Autoimmune thyroiditis 		G 0.700 GeneticVariation GWASCAT Seven newly identified loci for autoimmune thyroid disease. 22922229 2012