MIR646HG, MIR646 host gene, 284757

N. diseases: 5; N. variants: 6
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11700264
rs11700264
Entrez Id: 284757
Gene Symbol: MIR646HG
MIR646HG
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: rs164926
rs164926
Entrez Id: 284757
Gene Symbol: MIR646HG
MIR646HG
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: rs16983616
rs16983616
Entrez Id: 284757
Gene Symbol: MIR646HG
MIR646HG
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: rs16983616
rs16983616
Entrez Id: 284757
Gene Symbol: MIR646HG
MIR646HG
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: rs6027394
rs6027394
Entrez Id: 284757
Gene Symbol: MIR646HG
MIR646HG
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: rs1475029
rs1475029
Entrez Id: 284757;729296
Gene Symbol: MIR646HG;LOC729296
MIR646HG;LOC729296
CUI: C0008350
Disease:
Cholelithiasis 		0.700 GeneticVariation GWASDB A genome-wide association scan identifies the hepatic cholesterol transporter ABCG8 as a susceptibility factor for human gallstone disease. 17632509 2007
dbSNP: rs1475029
rs1475029
Entrez Id: 284757;729296
Gene Symbol: MIR646HG;LOC729296
MIR646HG;LOC729296
CUI: C0947622
Disease:
Cholecystolithiasis 		0.700 GeneticVariation GWASDB A genome-wide association scan identifies the hepatic cholesterol transporter ABCG8 as a susceptibility factor for human gallstone disease. 17632509 2007
dbSNP: rs6513497
rs6513497
Entrez Id: 284757;693231
Gene Symbol: MIR646HG;MIR646
MIR646HG;MIR646
CUI: C0279626
Disease:
Squamous cell carcinoma of esophagus 		0.010 GeneticVariation BEFREE To evaluate the association between mmSNPs and ESCC, a case-control study including 773 patients with ESCC and 882 gender- and age-matched controls was carried out to investigate the association of five mmSNPs (miR-449b rs10061133, miR-4293 rs12220909, miR-608 rs4919510, miR-627 rs2620381, and miR-646 rs6513497) with ESCC susceptibility. 26055141 2015