{"id":8162,"date":"2020-12-21T13:52:52","date_gmt":"2020-12-21T10:52:52","guid":{"rendered":"http:\/\/bgenz.com\/Bio\/product\/fto-a23525t-snp-screen-02-ml-tube-format-60-tests\/"},"modified":"2020-12-21T19:46:54","modified_gmt":"2020-12-21T16:46:54","slug":"fto-a23525t-snp-screen-02-ml-tube-format-60-tests","status":"publish","type":"product","link":"https:\/\/bgenz.com\/Bio\/product\/fto-a23525t-snp-screen-02-ml-tube-format-60-tests\/","title":{"rendered":"FTO (A23525T) SNP-Screen 0,2 ml tube format , 60 tests"},"content":{"rendered":"<p>A single nucleotide polymorphism (SNP pronounced &#8220;snip&#8221;) is a DNA polymorphisms at the level of a single nucleotide, a single base mutation in DNA. SNPs are \u2018conserved\u2019 across the genome and represent the most simple form and most common source of genetic polymorphism in the human genome: 90% of all human DNA polymorphisms are associated with SNPs and variation frequency is about 1 every 1000bp in the human genome (Sachidanandam et al.,2001).<\/p>\n<p>The SNPs in the genome can affect gene functions, protein structure or expression and for these reasons they are used as markers in genetic disease studies (Kim &#038; Mishra, 2007).<\/p>\n<p>It\u2019s sometimes possible to correlate a SNP with a particular trait or disease: susceptibility to disease may also be described as an \u2018unfortunate trait\u2019 that can be assessed checking if the mutated (unfortunate) polymorphism is carried in both alleles.<\/p>\n<p>SNPs testing can be applied to:<\/p>\n<p>Diagnostics \/ risk profiling<br \/>\nDrug response prediction<br \/>\nGene function identification<\/p>\n<p>Several SNPs have been associated to genetic susceptibility to different diseases and disorders like for example:<br \/>\n\u00b7         Hypertension<br \/>\n\u00b7         Fibrinolysis<br \/>\n\u00b7         Myocardial infarction<br \/>\n\u00b7         Ischemic stroke<br \/>\n\u00b7         Cancer<br \/>\n\u00b7         Metabolic disorders<\/p>\n","protected":false},"excerpt":{"rendered":"<p>RT-PCR test for detection of FTO gene mutation (rs9939609)<\/p>\n","protected":false},"featured_media":7830,"comment_status":"open","ping_status":"closed","template":"","meta":{"spay_email":""},"_links":{"self":[{"href":"https:\/\/bgenz.com\/Bio\/wp-json\/wp\/v2\/product\/8162"}],"collection":[{"href":"https:\/\/bgenz.com\/Bio\/wp-json\/wp\/v2\/product"}],"about":[{"href":"https:\/\/bgenz.com\/Bio\/wp-json\/wp\/v2\/types\/product"}],"replies":[{"embeddable":true,"href":"https:\/\/bgenz.com\/Bio\/wp-json\/wp\/v2\/comments?post=8162"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/bgenz.com\/Bio\/wp-json\/wp\/v2\/media\/7830"}],"wp:attachment":[{"href":"https:\/\/bgenz.com\/Bio\/wp-json\/wp\/v2\/media?parent=8162"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}