[\/et_pb_text][\/et_pb_column][\/et_pb_row][\/et_pb_section][et_pb_section fb_built=\u201d1\u2033 _builder_version=\u201d4.24.2\u2033 _module_preset=\u201ddefault\u201d custom_padding=\u201d10px||4px|||\u201d global_colors_info=\u201d{}\u201d][et_pb_row column_structure=\u201d1_4,3_4\u2033 _builder_version=\u201d4.25.1\u2033 _module_preset=\u201ddefault\u201d custom_margin=\u201d18px|auto||auto||\u201d animation_style=\u201dslide\u201d animation_direction=\u201dbottom\u201d global_colors_info=\u201d{}\u201d][et_pb_column type=\u201d1_4\u2033 _builder_version=\u201d4.25.1\u2033 _module_preset=\u201ddefault\u201d global_colors_info=\u201d{}\u201d][et_pb_image src=\u201dhttps: \/\/quimark.com\/wp-content\/uploads\/2024\/07\/family-scaled.jpg\u201d title_text=\u201dfamily\u201d _builder_version=\u201d4.27.0\u2033 _module_preset=\u201ddefault\u201d global_colors_info=\u201d{}\u201d][\/et_pb_image] [et_pb_image src=\u201dhttps:\/\/quimark.com\/wp-content\/uploads\/2024\/06\/MyRisk_Color-e1663713569913.png\u201d title_text=\u201dMyRisk_Color-e1663713569913\u2033 _builder_version=\u201d4.25.2\u2033 _module_preset=\u201ddefault\u201d width=\u201d100% \u201d global_colors_info=\u201d{}\u201d][\/et_pb_image][\/et_pb_column][et_pb_column type=\u201d3_4\u2033 _builder_version=\u201d4.25.1\u2033 _module_preset=\u201ddefault\u201d global_colors_info=\u201d{}\u201d][et_pb_text _builder_version=\u201d4.27.0 \u2033 text_font=\u201d|600|||||||\u201d text_text_color=\u201d#c8102e\u201d text_font_size=\u201d22px\u201d text_line_height=\u201d1.2em\u201d custom_margin=\u201d||-1px|||\u201d custom_padding=\u201d||17px|||\u201d global_colors_info=\u201d{}\u201d]<\/p>\n
Multigene Germline Testing for Hereditary Cancer<\/p>\n
[\/et_pb_text][et_pb_text _builder_version=\u201d4.27.0\u2033 text_font=\u201d||||||||\u201d text_text_color=\u201d#000000\u2033 text_font_size=\u201d17px\u201d text_line_height=\u201d1.8em\u201d ol_line_height=\u201d1.8em\u201d header_3_font=\u201d|700|||||||\u201d header_3_font_size=\u201d23px\u201d header_3_line_height=\u201d1.5em\u201d custom_margin=\u201d-10px|||||\u201d custom_padding=\u201d|0px||||\u201d link_option_url_new_window=\u201don\u201d global_colors_info=\u201d{}\u201d]<\/p>\n
<\/p>\n
MyRisk Plus Utilities<\/h3>\n
MyRisk is a multigene germline blood test that can help determine a patient's hereditary cancer risk by focusing on eleven of the most common hereditary cancers.<\/p>\n
Which genes are tested?<\/h3>\n
Here are the 48 genes analyzed by MyRisk Plus.\u00a0<\/span><\/p>\n Genetic mutations passed down from parents can dramatically increase the risk of disease, including many types of cancer. In fact, patients with some rare inherited cancer syndromes may have up to a 100% chance of developing certain types of cancer.<\/p>\n The ongoing discovery of genes involved in cancer allows us to test for cancer-causing mutations in these genes, which may increase the risk of cancer.<\/p>\n If a patient has a mutation that puts them at increased risk for cancer, there are steps you can take to help reduce their risk through increased surveillance, chemoprevention, prophylactic surgery, and risk counseling.<\/p>\n Identifying your potential cancer risk is the first step in determining how best to delay, or even prevent, the development of certain cancers.<\/p>\n The MyRisk test is intended for both women and men. Individuals with a familial or inherited risk of cancer are much more likely to develop cancer during their lifetime.<\/p>\n A blood sample is sent\u00a0<\/span>to Myriad Genetics laboratories in the USA where it is <\/span>performed the MyRisk Plus test in a few days.\u00a0 \u00a0<\/span><\/p>\n The test must be requested by the attending physician, who will have access to the patient's report via the Myriad Genetics secure computing platform.\u00a0<\/span><\/p>\n <\/span><\/p>\n The MyRisk Germline Test evaluates 48 genes linked to one or more of 11 tumor sites. Results will list the specific mutations found, including variants of uncertain significance (VUS). A summary of medical society guidelines is also provided to guide and optimize treatment decisions in MyRiskManagementTool<\/em> (MMT).<\/span><\/p>\n <\/p>\n A mutation has been identified.<\/p>\n<\/div>\n A high risk has been identified.<\/p>\n<\/div>\n No clinically significant mutations.<\/p>\n<\/div>\n An undetermined risk mutation has been identified.<\/p>\n<\/div>\n<\/div>\n <\/p>\n <\/p>\n <\/p>\n [\/et_pb_text][\/et_pb_column][\/et_pb_row][\/et_pb_section][et_pb_section fb_built=\u201d1\u2033 admin_label=\u201ds\u201d _builder_version=\u201d4.25.2\u2033 background_color=\u201d#002855\u2033 custom_padding=\u201d0px||110px||false |false\u201d box_shadow_style=\u201dpreset7\u2033 box_shadow_horizontal=\u201d0px\u201d box_shadow_vertical=\u201d100px\u201d box_shadow_color=\u201d#ffffff\u201d global_module=\u201d51463\u2033 saved_tabs=\u201dall\u201d global_colors_info=\u201d{}\u201d][et_pb_row column_structure=\u201d1_3,1_3,1_3 \u2033 padding_top_bottom_link_1=\u201dtrue\u201d 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header_2_font_size_last_edited=\u201don|phone\u201d global_colors_info=\u201d{}\u201d]<\/p>\n [\/et_pb_text][et_pb_blurb title=\u201dTelephone\u201d use_icon=\u201don\u201d font_icon=\u201d\ue090||divi||400\u2033 icon_color=\u201d#ffffff\u201d icon_placement=\u201dleft\u201d image_icon_width=\u201d28px\u201d _builder_version=\u201d4.27.0\u2033 header_font =\u201d|600|||||||\u201d header_text_color=\u201d#ffffff\u201d header_font_size=\u201d20px\u201d header_line_height=\u201d1.2em\u201d body_font=\u201d||||||||\u201d body_text_color=\u201d#ffffff\u201d body_font_size=\u201d15px\u201d body_line_height=\u201d1.8em\u201d background_layout=\u201ddark\u201d custom_padding=\u201d15px|||\u201d animation_direction=\u201dleft\u201d animation=\u201doff\u201d header_font_size_tablet=\u201d\u201d header_font_size_phone=\u201d18px\u201d header_font_size_last_edited=\u201don|phone\u201d icon_font_size=\u201d28px\u201d global_colors_info=\u201d{}\u201d]<\/p>\n +39 0239261913<\/p>\n [\/et_pb_blurb][et_pb_blurb title=\u201dEmail\u201d use_icon=\u201don\u201d font_icon=\u201d\ue076||divi||400\u2033 icon_color=\u201d#ffffff\u201d icon_placement=\u201dleft\u201d image_icon_width=\u201d28px\u201d _builder_version=\u201d4.27.0\u2033 header_font =\u201d|600|||||||\u201d header_text_color=\u201d#ffffff\u201d header_font_size=\u201d20px\u201d header_line_height=\u201d1.2em\u201d body_font=\u201d|600|||||||\u201d body_text_color=\u201d#ffffff\u201d body_font_size=\u201d15px\u201d body_line_height=\u201d1.8em\u201d background_layout=\u201ddark\u201d custom_padding=\u201d15px|||\u201d animation_direction=\u201dleft\u201d animation=\u201doff\u201d header_font_size_tablet=\u201d\u201d header_font_size_phone=\u201d18px\u201d header_font_size_last_edited=\u201don|phone\u201d icon_font_size=\u201d28px\u201d global_colors_info=\u201d{}\u201d]<\/p>\n info@quimark.com<\/p>\n [\/et_pb_blurb][\/et_pb_column][et_pb_column type=\u201d1_3\u2033 _builder_version=\u201d4.27.0\u2033 background_color=\u201d#c8102e\u201d background_color_gradient_direction=\u201d190deg\u201d background_color_gradient_start=\u201d#3fa2f7\u2033 background_color_gradient_start_position=\u201d8 5%\u201d background_color_gradient_end=\u201drgba(255,255,255,0 )\u201d background_color_gradient_end_position=\u201d0%\u201d custom_padding=\u201d40px|70px|200px|70px|false|false\u201d custom_padding_tablet=\u201d|10%||10%||true\u201d custom_padding_phone=\u201d||160px||false|true\u201d custom_padding_last_edited=\u201don|phone\u201d global_colors_info=\u201d{}\u201d custom_padding__hover=\u201d|||\u201d][et_pb_text _builder_version=\u201d4.27.0\u2033 _module_preset=\u201ddefault\u201d min_height=\u201d 771px\u201d custom_margin=\u201d||-1085px|||\u201d custom_padding=\u201d0px||56px|0px||\u201d global_colors_info=\u201d{}\u201d]<\/p>\n The content of this website is informative about the Quimark company and its products and services, [\/et_pb_text][et_pb_blurb icon_placement=”left” 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%%Oggetto%%||et_pb_line_break_holder||Messaggio: %%Messaggio%%||et_pb_line_break_holder||||et_pb_line_break_holder||x Acconsento al trattamento dei miei dati personali come espresso nella privacy policy del sito web.” submit_button_text=”Invia Messaggio” module_id=”et_pb_contact_form_0″ _builder_version=”4.27.0″ form_field_background_color=”#FFFFFF” form_field_text_color=”#000000″ title_font=”|700||on|||||” title_text_color=”#ffffff” title_font_size=”30px” title_line_height=”1.6em” form_field_font=”Roboto|300|||||||” form_field_font_size=”14px” form_field_line_height=”1.6em” custom_button=”on” button_text_size=”14px” button_text_color=”#000000″ button_bg_color=”#ffffff” button_border_width=”12px” button_border_color=”#ffffff” button_border_radius=”0px” button_letter_spacing=”1px” button_font=”|600||on|||||” button_use_icon=”off” animation_direction=”top” title_font_size_tablet=”” title_font_size_phone=”22px” title_font_size_last_edited=”on|phone” border_width_all=”1px” 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%22,%22checked%22:0,%22dragID%22:-1,%22link_url%22:%22https:\/\/quimark.com\/privacy-policy\/%22,%22link_text%22:%22privacy policy%22}%93″ fullwidth_field=”on” _builder_version=”4.25.2″ _module_preset=”default” global_colors_info=”{}”][\/et_pb_contact_field][\/et_pb_contact_form][\/et_pb_column][\/et_pb_row][\/et_pb_section]<\/p>","protected":false},"excerpt":{"rendered":" MyRisk\u00ae PlusMultigene Germline Test for Hereditary Cancer How does MyRisk Plus help? MyRisk is a multigene germline blood test that can help determine a patient\u2019s hereditary cancer risk by focusing on eleven of the most common hereditary cancers. Which genes are tested? Here are the 48 genes MyRisk Plus tests. Predicting a disease Mutations [\u2026]<\/p>","protected":false},"author":4,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_et_pb_use_builder":"on","_et_pb_old_content":"","_et_gb_content_width":"","footnotes":""},"categories":[13],"tags":[],"class_list":["post-51839","post","type-post","status-publish","format-standard","hentry","category-prodotti"],"yoast_head":"\n![\"\"](\"https:\/\/quimark.com\/wp-content\/uploads\/2024\/06\/GeneTable_page-0001-1024x791.jpg\")
<\/p>\nPredicting a disease<\/h3>\n
<\/h3>\n
Act consciously<\/h3>\n
<\/h3>\n
Who is MyRisk Plus for?<\/h3>\n
If a patient has a personal or family history of cancer, hereditary cancer testing is the only way to determine whether that patient has a hereditary, familial, or general risk of developing future cancer.<\/p>\nHow do I use MyRisk Plus?<\/h3>\n
![\"\"](\"https:\/\/quimark.com\/wp-content\/uploads\/2024\/05\/MyRisk_STS_BOX_14_03_23_EN_REND3D-2.png\")
<\/span><\/p>\nThe Report: MyRisk Plus provides clear and reliable results<\/h3>\n
![\"\"](\"https:\/\/quimark.com\/wp-content\/uploads\/2024\/08\/MyRisk-report-JPG-cornice-233x300.jpg\")
<\/a><\/p>\n![\"Positive](\"https:\/\/myriad.com\/wp-content\/uploads\/2023\/01\/positive-icon-red.svg\"){kind=icon}
Positive Result<\/strong><\/p>\n![\"Elevated](\"https:\/\/myriad.com\/wp-content\/uploads\/2023\/01\/eleveated-icon-orange.svg\"){kind=icon}
High Result\u00a0<\/strong><\/div>\n![\"Negative](\"https:\/\/myriad.com\/wp-content\/uploads\/2023\/01\/negative-icon-green.svg\"){kind=icon}
Negative Result<\/strong><\/div>\n![\"Variant](\"https:\/\/myriad.com\/wp-content\/uploads\/2023\/01\/VUS-icon-gray.svg\"){kind=icon}
Variant of Uncertain Meaning<\/strong>
(Variant of Uncertain Significance<\/em>( (VUS)<\/div>\nTechnical Test Specifications (in English)<\/a><\/h3>\n
![\"\"](\"https:\/\/quimark.com\/wp-content\/uploads\/2024\/08\/MyRiskPlusEuropeTechnicalSpecifications-JPG-cornice-2-233x300.jpg\")
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More information\u00a0<\/a><\/h3>\n
For information<\/span><\/h2>\n
<\/span>It is not intended as professional medical or health advice.<\/span><\/p>\n