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SNP information rs2107595

RS2107595

Normal allele: GG

HDAC9 Rs2107595 variant alters susceptibility to coronary heart disease and severity of coronary atherosclerosis.

Polymorphism rs2107595 is related to topics like this:

Heart disease genetic

Although genetics can be a major factor in the development of certain heart diseases, individuals...

Stroke genes

Ischemic stroke has a multifactorial etiology, with genetic causes playing a significant role,...


Research and publications:

  23449258   Evidence HDAC9 genetic variant associated with ischemic stroke increases risk via promoting carotid atherosclerosis.

  25388417   Deficiency of the stroke relevant HDAC9 gene attenuates atherosclerosis in accord with allele-specific effects at 7p21.1.

  26093197   Association of GWAS-supported loci rs2107595 in HDAC9 gene with ischemic stroke in southern Han Chinese.

  26892960   From Loci to Biology: Functional Genomics of Genome-Wide Association for Coronary Disease.

  26935894   Low-frequency and common genetic variation in ischemic stroke: The METASTROKE collaboration.

  27494404   HDAC9 Variant Rs2107595 Modifies Susceptibility to Coronary Artery Disease and the Severity of Coronary Atherosclerosis in a Chinese Han Population.

  27642596   Polymorphism of HDAC9 Gene Is Associated with Increased Risk of Acute Coronary Syndrome in Chinese Han Population.

  27796860   Genetic Risk Factors for Ischemic and Hemorrhagic Stroke.

  28145521   The association between HDAC9 gene polymorphisms and stroke risk in the Chinese population: A meta-analysis.

  28975602   APOL1, CDKN2A/CDKN2B, and HDAC9 polymorphisms and small vessel ischemic stroke.

  29273593   Novel Susceptibility Loci for Moyamoya Disease Revealed by a Genome-Wide Association Study.

  29390587   Prospective association of a genetic risk score with major adverse cardiovascular events in patients with coronary artery disease.

  29651704   HDAC9 Polymorphism Alters Blood Gene Expression in Patients with Large Vessel Atherosclerotic Stroke.

  29695241   Novel risk genes identified in a genome-wide association study for coronary artery disease in patients with type 1 diabetes.

  31500558   The Atherosclerosis Risk Variant rs2107595 Mediates Allele-Specific Transcriptional Regulation of HDAC9 via E2F3 and Rb1.

  31757599   Ischemic Stroke and Genetic Variants: In Search of Association with Severity and Recurrence in a Brazilian Population.

  31917787   Genomic profiling of human vascular cells identifies TWIST1 as a causal gene for common vascular diseases.

  32284067   Association between rs2107595 HDAC9 gene polymorphism and advanced carotid atherosclerosis in the Slovenian cohort.

  34150032   GWAS-linked hot loci predict short-term functional outcome and recurrence of ischemic stroke in Chinese population.

  35124268   Mendelian Randomization Analysis Reveals No Causal Relationship Between Nonalcoholic Fatty Liver Disease and Severe COVID-19.

  35379196   Analysis of 61 SNPs from the CAD specific genomic loci reveals unique set of SNPs as significant markers in the Southern Indian population of Hyderabad.

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