{"version":"1.0","provider_name":"Center for Inherited Oncogenesis","provider_url":"https:\/\/wp.uthscsa.edu\/cio","title":"Identifying Genetic Variants Associated with Cancer Risk - Center for Inherited Oncogenesis","type":"rich","width":600,"height":338,"html":"<blockquote class=\"wp-embedded-content\" data-secret=\"0FdG0vXJqN\"><a href=\"https:\/\/wp.uthscsa.edu\/cio\/research\/identifying-genetic-variants\/\">Identifying Genetic Variants Associated with Cancer Risk<\/a><\/blockquote><iframe sandbox=\"allow-scripts\" security=\"restricted\" src=\"https:\/\/wp.uthscsa.edu\/cio\/research\/identifying-genetic-variants\/embed\/#?secret=0FdG0vXJqN\" width=\"600\" height=\"338\" title=\"&#8220;Identifying Genetic Variants Associated with Cancer Risk&#8221; &#8212; Center for Inherited Oncogenesis\" data-secret=\"0FdG0vXJqN\" frameborder=\"0\" marginwidth=\"0\" marginheight=\"0\" scrolling=\"no\" class=\"wp-embedded-content\"><\/iframe><script>\n\/*! This file is auto-generated *\/\n!function(d,l){\"use strict\";l.querySelector&&d.addEventListener&&\"undefined\"!=typeof URL&&(d.wp=d.wp||{},d.wp.receiveEmbedMessage||(d.wp.receiveEmbedMessage=function(e){var t=e.data;if((t||t.secret||t.message||t.value)&&!\/[^a-zA-Z0-9]\/.test(t.secret)){for(var s,r,n,a=l.querySelectorAll('iframe[data-secret=\"'+t.secret+'\"]'),o=l.querySelectorAll('blockquote[data-secret=\"'+t.secret+'\"]'),c=new RegExp(\"^https?:$\",\"i\"),i=0;i<o.length;i++)o[i].style.display=\"none\";for(i=0;i<a.length;i++)s=a[i],e.source===s.contentWindow&&(s.removeAttribute(\"style\"),\"height\"===t.message?(1e3<(r=parseInt(t.value,10))?r=1e3:~~r<200&&(r=200),s.height=r):\"link\"===t.message&&(r=new URL(s.getAttribute(\"src\")),n=new URL(t.value),c.test(n.protocol))&&n.host===r.host&&l.activeElement===s&&(d.top.location.href=t.value))}},d.addEventListener(\"message\",d.wp.receiveEmbedMessage,!1),l.addEventListener(\"DOMContentLoaded\",function(){for(var e,t,s=l.querySelectorAll(\"iframe.wp-embedded-content\"),r=0;r<s.length;r++)(t=(e=s[r]).getAttribute(\"data-secret\"))||(t=Math.random().toString(36).substring(2,12),e.src+=\"#?secret=\"+t,e.setAttribute(\"data-secret\",t)),e.contentWindow.postMessage({message:\"ready\",secret:t},\"*\")},!1)))}(window,document);\n\/\/# sourceURL=https:\/\/wp.uthscsa.edu\/cio\/wp-includes\/js\/wp-embed.min.js\n<\/script>\n","description":"[vc_row][vc_column width=&#8221;2\/3&#8243;][vc_column_text css=&#8221;&#8221;]Two different types of DNA risk variants for cancer have so far been identified: Rare, high or moderate risk protein coding variants that affect disease risk through their direct interaction with specific pathways that drive cancer pathogenesis. Identifying these variants or mutations in subjects before they get cancer is a major aspect of [&hellip;]"}