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Ischemic heart disease DNA health report

Follow the link of the selected polymorphism to read a brief description of how the selected polymorphism affects Ischemic heart disease and see a list of existing studies.

SNP polymorphisms related to the topic Ischemic heart disease:

rs671A mutation in the mitochondrial aldehyde dehydrogenase (ALDH2) gene increases acute alcohol sensitivity, alcohol dependence and hangover susceptibility.
rs3803
rs5443
rs20455
rs46522The rs46522 polymorphism of the E2Z ubiquitin-conjugating enzyme gene is associated with abnormal metabolic parameters in patients with myocardial infarction.
rs383830Male-specific association of the T allele of APC rs383830 with risk of coronary heart disease.
rs501120
rs514659
rs556621The rs556621 variant on chromosome 6p21.1 is associated with large artery atherosclerotic stroke and ischaemic stroke.
rs579459
rs599839The rs599839 polymorphism on chromosome 1p13.3 is associated with premature coronary heart disease.
rs646776A new locus of coronary atherosclerosis and associations with myocardial infarction in coronary atherosclerosis.
rs662799Apolipoprotein A5 polymorphisms increase 1.4-fold the risk of early heart attack.
rs675026
rs688034
rs703752
rs708272
rs879324Genetic risk factor for ischaemic and haemorrhagic stroke.
rs886126
rs964184Involved in lipid and vitamin E metabolism. The genotype is a moderate risk factor for reduced vitamin E levels. A low-fat diet is suitable for people with this defect. On a low-fat diet (20% of energy comes from fat), carriers of the risk allele (allele G) had greater reductions in OX and LDL cholesterol levels. These studies showed better lipid profile improvement with long-term low-fat dietary intake in the risk allele G.
rs974819
rs1024611Increased risk of exercise-induced ischaemia. Also increased rate of HIV progression.
rs1063192
rs1165669
rs1231206
rs1263173
rs1333040
rs1333042Intronic polymorphisms in the CDKN2B-AS1 gene are strongly associated with the risk of myocardial infarction and coronary heart disease.
rs1333048ANRIL genetic variation is strongly associated with the risk of myocardial infarction and coronary heart disease.
rs1333049
rs1412444A single nucleotide polymorphism in the LIPA (lysosomal acidic lipase A) gene is associated with predisposition to premature coronary heart disease.
rs1676232LSAMP tumour suppressor gene polymorphisms define a significant risk haplotype for left main artery coronary heart disease.
rs1746048
rs1799983Decreases the activity of the NOS3 gene and may reduce the efficiency of the methylation process. Also associated with increased risk markers for cardiovascular problems, such as total cholesterol and low-density lipoprotein (LDL) levels, and with an increased risk of high blood pressure, especially in pregnant women.
rs1800787
rs1842896
rs1994016
rs2107595HDAC9 Rs2107595 variant alters susceptibility to coronary heart disease and severity of coronary atherosclerosis.
rs2123536
rs2238151
rs2259816
rs2306374
rs2331291
rs2346177
rs2383206
rs2383207
rs2472299
rs2505083Increased risk of sudden myocardial infarction and coronary heart disease.
rs2515629
rs2713604
rs2811712
rs2857657
rs2895811HHIPL-1 gene polymorphism (rs2895811) is associated with cardiovascular risk factors and cardiometabolic parameters in patients with myocardial infarction.
rs2943634
rs3127599
rs3135506A variant of the apolipoprotein A5 gene affects lipids, lipoproteins and is associated with coronary heart disease.
rs3729639
rs3782218A single nucleotide polymorphism of nitric oxide synthase (NOS) is associated with coronary heart disease.
rs3798220rs3798220, also known as I4399M or Ile4399Met, is a SNP in the apolipoprotein (A) LPA gene , which has been reported to be associated with elevated plasma lipoprotein levels and increased cardiovascular risk, well-tolerated by low-dose aspirin.
rs3869109
rs3918242
rs4404477
rs4665058There is an approximately 4-fold increased risk of sudden cardiac death, presumably from myocardial infarction.
rs4743150
rs4773144
rs4977574
rs6504218
rs6601299
rs6725887
rs6843082Genetic risk factor for ischaemic and haemorrhagic stroke.
rs6882776
rs6905288
rs6922269
rs7025486
rs7136259
rs7203193
rs7250581
rs7569328
rs7586970
rs7697839
rs7767084
rs7808424
rs8055236
rs8060686
rs9268402
rs9349379
rs9546711
rs9818870
rs9982601
rs10116277
rs10455872The rs10455872(G) allele of the LPA gene is associated with high levels of lipoprotein and elevated calcium in the aortic valve, coronary artery disease and coronary heart disease.
rs10755578
rs10757274A genetic variant on chromosome 9p21 is the strongest genetic predictor of early myocardial infarction (heart attack) found so far. SNPs in this region are also associated with an increased risk of stroke, abdominal aortic aneurysm (AAA) and intracranial aneurysm.
rs10757278
rs10933436
rs10953541
rs11066015
rs11066280
rs11206510
rs11556924
rs11650066
rs11669133
rs11671653
rs11752643
rs11984041HDAC9 variant associated with large vessel ischaemic stroke contributes to carotid atherosclerosis.
rs12190287
rs12200560
rs12413409
rs12425791NINJ2 promoter polymorphism causes association with ischaemic stroke.
rs12526453
rs12740374
rs12936587
rs13407662
rs16851055
rs17114036
rs17114046
rs17228212
rs17465637SNP of the MIA3 gene associated with increased risk of myocardial infarction with odds ratios of 1.17 (CI: 1.04-1.32) and 1.37 (CI: 1.08-1.74) for carriers.
rs17672135
rs28936670
rs72554028
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