[vc_row full_width=”stretch_row_content_no_spaces” css=”.vc_custom_1465208345334{padding-top: 0px !important;padding-bottom: 0px !important;}”][vc_column width=”1/4″ bgcolor=”dark” css=”.vc_custom_1473413359671{padding-top: 60px !important;padding-right: 40px !important;padding-bottom: 40px !important;padding-left: 40px !important;background-image: url(https://b3075120.smushcdn.com/3075120/wp-content/uploads/2016/06/data-img-2.png?lossy=1&strip=1&webp=1) !important;background-position: center !important;background-repeat: no-repeat !important;background-size: cover !important;}”][tm-servicebox h2=”CANCER PANEL 1″ txt_align=”left” add_icon=”left” i_icon_fontawesome=”fas fa-vial” i_color=”white” i_background_style=”none” i_size=”lg” h4=”(88 GENES)”][/tm-servicebox][/vc_column][vc_column width=”1/4″ bgcolor=”skin” css=”.vc_custom_1588155568003{padding-top: 60px !important;padding-right: 40px !important;padding-bottom: 40px !important;padding-left: 40px !important;background-image: url(https://b3075120.smushcdn.com/3075120/wp-content/uploads/2016/09/data-img-1.png?lossy=1&strip=1&webp=1) !important;background-position: center !important;background-repeat: no-repeat !important;background-size: cover !important;}”][tm-servicebox h2=”CANCER PANEL 2″ txt_align=”left” add_icon=”left” i_icon_fontawesome=”fas fa-vial” i_color=”white” i_background_style=”none” i_size=”lg” css=”.vc_custom_1593575677723{background-position: center !important;background-repeat: no-repeat !important;background-size: cover !important;}” h4=”(171 GENES)”][/tm-servicebox][/vc_column][vc_column width=”1/4″ bgcolor=”dark” css=”.vc_custom_1473413875162{padding-top: 60px !important;padding-right: 40px !important;padding-bottom: 40px !important;padding-left: 40px !important;background-image: url(https://b3075120.smushcdn.com/3075120/wp-content/uploads/2016/06/data-img-4.png?lossy=1&strip=1&webp=1) !important;background-position: center !important;background-repeat: no-repeat !important;background-size: cover !important;}”][tm-servicebox h2=”CANCER MASTER PANEL” txt_align=”left” add_icon=”left” i_icon_fontawesome=”fas fa-vial” i_color=”white” i_background_style=”none” i_size=”lg” css=”.vc_custom_1593575691849{background-position: center !important;background-repeat: no-repeat !important;background-size: cover !important;}” h4=”(546 GENES)”][/tm-servicebox][/vc_column][vc_column width=”1/4″ textcolor=”dark” bgcolor=”skin” css=”.vc_custom_1588155722874{padding-top: 60px !important;padding-right: 40px !important;padding-bottom: 40px !important;padding-left: 40px !important;background-image: url(https://b3075120.smushcdn.com/3075120/wp-content/uploads/2020/04/image.img_.jpeg?lossy=1&strip=1&webp=1) !important;background-position: center !important;background-repeat: no-repeat !important;background-size: cover !important;}”][tm-servicebox h2=”BRCA LITE” txt_align=”left” add_icon=”left” i_icon_fontawesome=”fas fa-vial” i_color=”white” i_background_style=”none” i_size=”lg” css=”.vc_custom_1593575715288{background-position: center !important;background-repeat: no-repeat !important;background-size: cover !important;}” h4=”.”][/tm-servicebox][/vc_column][/vc_row][vc_row css=”.vc_custom_1466684306569{padding-bottom: 70px !important;}”][vc_column width=”1/2″ css=”.vc_custom_1466684143452{padding-top: 40px !important;}”][vc_custom_heading text=”AXEN” font_container=”tag:h2|font_size:24px|text_align:left|color:%23222222|line_height:30px” google_fonts=”font_family:Ubuntu%3A300%2C300italic%2Cregular%2Citalic%2C500%2C500italic%2C700%2C700italic|font_style:500%20bold%20regular%3A500%3Anormal”][vc_custom_heading text=”Macrogen BRCA1/2″ font_container=”tag:h3|font_size:18px|text_align:left|color:rgba(34%2C34%2C34%2C0.73)|line_height:24px” google_fonts=”font_family:Ubuntu%3A300%2C300italic%2Cregular%2Citalic%2C500%2C500italic%2C700%2C700italic|font_style:500%20bold%20regular%3A500%3Anormal”][vc_column_text]Macrogen BRCA1/2 testing is a next-generation sequencing test that searches for mutation in BRCA1 and BRCA2 genes. It is best suited for individuals with either a history of early onset breast or ovarian cancer or a strong family history of breast and/or ovarian cancer.

Cancers occur due to various causes, but some cancers are caused by genetic mutations of specific inherited genes. People who have such cancer-related mutations have far more risk of cancer than others. Hereditary cancers are caused by gene abnormalities inherited from parents, and the incidence of cancer in the same family is high. Thus, early detection and identification of the exact cause through gene diagnosis is required.[/vc_column_text][vc_btn title=”Know more” style=”classic” link=”url:https%3A%2F%2Fweb.facebook.com%2Fmacrogenoncology%2F|||”][/vc_column][vc_column width=”1/2″][vc_gallery interval=”3″ images=”4445,4442″ img_size=”large”][/vc_column][/vc_row][vc_row][vc_column][clients title=”” heading_sep=”no” show=”4″ column=”four”][/vc_column][/vc_row]