Cancer Genetic Testing From Home

Statistics

In the UK, 1 in 2 people will be diagnosed with cancer at some point in their life. Genetic testing can help identify your risk of developing some of the most common types of cancer, so you can take action early.

Up to 10%

of all cancers are linked to inherited genetic changes — including some of the most common gender-specific cancers like breast cancer and prostate cancer.

Genetic Counselling

The Power of Pedigree

A key part of your test is a 45-minute personalised session with one of our genetic counsellors. Genetics can be complex, but you're not alone—we're here to guide you through it. By exploring your family history, we can uncover valuable insights that could make a real difference to your health.

The Test

Cancer Focus Panel

Our genetic cancer panel focuses on 50 carefully chosen genes, all backed by strong scientific evidence. While some tests look at more genes, many include ones with little clinical value. We focus on what’s most useful—so you get results you can actually act on.

The Lab

Fulgent Genetics - Trusted Partner

Fulgent Genetics, based in California, is a global leader in genetic testing and analysis. We’ve partnered with them because quality matters—especially when it comes to your health. Their state-of-the-art Illumina sequencing technology delivers over 99% accuracy at 50x coverage, ensuring your results are both reliable and clinically meaningful.

Research

World-class experts

Medicine is always evolving—and so are we. Our expert team stays up to date with the latest research and clinical guidelines, so you’re always getting advice that’s current, trusted, and tailored to you.

Gene List

Learn about our carefully selected list of
genes relating to higher cancer risk

Gene Group	Genes	Associated Cancers
DNA Mismatch Repair (MMR)	MLH1, MSH2, MSH6, PMS2, EPCAM, MSH3, MLH3	Colorectal, endometrial, ovarian, gastric, small-intestine, urinary-tract
Homologous Recombination Repair (HRR)	BRCA1, BRCA2, PALB2, ATM, CHEK2, RAD51C, RAD51D, BARD1, BRIP1	Breast, ovarian, pancreatic, prostate, gastric, other solid tumors
Adenomatous & Polyposis Genes	APC, MUTYH, AXIN2, RNF43, GREM1, BMPR1A, SMAD4	Colorectal adenomas & carcinoma; duodenal/jejunal & gastric polyps
Polymerase-Proofreading Polyposis	POLE, POLD1	Colorectal adenomas & carcinoma; endometrial carcinoma
Base Excision Repair (BER)	NTHL1, MBD4	Colorectal adenomas & carcinoma; acute myeloid leukemia
Other High-Penetrance Syndromes	TP53, CDH1, PTEN, STK11	Sarcoma, breast, brain, adrenocortical; diffuse gastric, lobular breast; Cowden: breast, thyroid, endometrial; PJS: pancreatic, GI, lung
Renal-Cancer Predisposition	VHL, MET, FH, FLCN	Clear-cell RCC, papillary RCC, leiomyomatosis-RCC, chromophobe RCC; hemangioblastomas, pheochromocytomas, lung cysts
Endocrine Tumor Syndromes	MEN1, RET, CDKN1B	Parathyroid, pituitary, pancreatic endocrine; medullary thyroid carcinoma; pheochromocytoma
Neurocutaneous Tumor Syndromes	NF1, TSC1, TSC2	Neurofibromas, MPNST, glioma; SEGAs, renal angiomyolipomas
Paraganglioma/Pheochromocytoma Genes	SDHA, SDHB, SDHC, SDHD, TMEM127, MAX	Paragangliomas, pheochromocytomas, occasionally GIST
Other Cancer Predisposition	CDKN2A, BAP1, HOXB13	Melanoma, pancreatic; mesothelioma, uveal melanoma, RCC; hereditary prostate cancer

Gene Group	Genes	Associated Cancers
DNA Mismatch Repair (MMR)	MLH1, MSH2, MSH6, PMS2, EPCAM, MSH3, MLH3	Colorectal, endometrial, ovarian, gastric, small-intestine, urinary-tract
Homologous Recombination Repair (HRR)	BRCA1, BRCA2, PALB2, ATM, CHEK2, RAD51C, RAD51D, BARD1, BRIP1	Breast, ovarian, pancreatic, prostate, gastric, other solid tumors
Adenomatous & Polyposis Genes	APC, MUTYH, AXIN2, RNF43, GREM1, BMPR1A, SMAD4	Colorectal adenomas & carcinoma; duodenal/jejunal & gastric polyps
Polymerase-Proofreading Polyposis	POLE, POLD1	Colorectal adenomas & carcinoma; endometrial carcinoma
Base Excision Repair (BER)	NTHL1, MBD4	Colorectal adenomas & carcinoma; acute myeloid leukemia
Other High-Penetrance Syndromes	TP53, CDH1, PTEN, STK11	Sarcoma, breast, brain, adrenocortical; diffuse gastric, lobular breast; Cowden: breast, thyroid, endometrial; PJS: pancreatic, GI, lung
Renal-Cancer Predisposition	VHL, MET, FH, FLCN	Clear-cell RCC, papillary RCC, leiomyomatosis-RCC, chromophobe RCC; hemangioblastomas, pheochromocytomas, lung cysts
Endocrine Tumor Syndromes	MEN1, RET, CDKN1B	Parathyroid, pituitary, pancreatic endocrine; medullary thyroid carcinoma; pheochromocytoma
Neurocutaneous Tumor Syndromes	NF1, TSC1, TSC2	Neurofibromas, MPNST, glioma; SEGAs, renal angiomyolipomas
Paraganglioma/Pheochromocytoma Genes	SDHA, SDHB, SDHC, SDHD, TMEM127, MAX	Paragangliomas, pheochromocytomas, occasionally GIST
Other Cancer Predisposition	CDKN2A, BAP1, HOXB13	Melanoma, pancreatic; mesothelioma, uveal melanoma, RCC; hereditary prostate cancer

DNA Mismatch Repair (MMR)

Genes:

MLH1, MSH2, MSH6, PMS2, EPCAM, MSH3, MLH3

Associated Cancers:

Colorectal, endometrial, ovarian, gastric, small-intestine, urinary-tract

Homologous Recombination Repair (HRR)

Genes:

BRCA1, BRCA2, PALB2, ATM, CHEK2, RAD51C, RAD51D, BARD1, BRIP1

Associated Cancers:

Breast, ovarian, pancreatic, prostate, gastric, other solid tumors

Adenomatous & Polyposis Genes

Genes:

APC, MUTYH, AXIN2, RNF43, GREM1, BMPR1A, SMAD4

Associated Cancers:

Colorectal adenomas & carcinoma; duodenal/jejunal & gastric polyps

Polymerase-Proofreading Polyposis

Genes:

POLE, POLD1

Associated Cancers:

Colorectal adenomas & carcinoma; endometrial carcinoma

Base Excision Repair (BER)

Genes:

NTHL1, MBD4

Associated Cancers:

Colorectal adenomas & carcinoma; acute myeloid leukemia

Other High-Penetrance Syndromes

Genes:

TP53, CDH1, PTEN, STK11

Associated Cancers:

Sarcoma, breast, brain, adrenocortical; diffuse gastric, lobular breast; Cowden: breast, thyroid, endometrial; PJS: pancreatic, GI, lung

Renal-Cancer Predisposition

Genes:

VHL, MET, FH, FLCN

Associated Cancers:

Clear-cell RCC, papillary RCC, leiomyomatosis-RCC, chromophobe RCC; hemangioblastomas, pheochromocytomas, lung cysts

Endocrine Tumor Syndromes

Genes:

MEN1, RET, CDKN1B

Associated Cancers:

Parathyroid, pituitary, pancreatic endocrine; medullary thyroid carcinoma; pheochromocytoma

Neurocutaneous Tumor Syndromes

Genes:

NF1, TSC1, TSC2

Associated Cancers:

Neurofibromas, MPNST, glioma; SEGAs, renal angiomyolipomas

Paraganglioma/Pheochromocytoma Genes

Genes:

SDHA, SDHB, SDHC, SDHD, TMEM127, MAX

Associated Cancers:

Paragangliomas, pheochromocytomas, occasionally GIST

Other Cancer Predisposition

Genes:

CDKN2A, BAP1, HOXB13

Associated Cancers:

Melanoma, pancreatic; mesothelioma, uveal melanoma, RCC; hereditary prostate cancer

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CancerGenetic Testing

Type of Cancers

Breast Cancer

Ovarian Cancer

Prostate Cancer

Pancreatic Cancer

Colorectal Cancer

Melanoma

Kidney Cancer

Endometrial Cancer

Nervous System Tumors

Stomach Cancer

Retinoblastoma

Lobular Breast Cancer

Brain Cancer

Leukemia

Thyroid cancer

Lymphoma

Adrenal Gland Tumors

Cervical Cancer

Sarcomas

Lung Cancer

Type of Cancers

Type of Cancers

Breast Cancer

Ovarian Cancer

Prostate Cancer

Pancreatic Cancer

Colorectal Cancer

Nervous System Tumors

Stomach Cancer

Endometrial Cancer

Retinoblastoma

Lobular Breast Cancer

Brain Cancer

Leukemia

Thyroid cancer

Melanoma

Lymphoma

Adrenal Gland Tumors

Kidney cancer

Cervical Cancer

Sarcomas

Lung Cancer

Statistics

In the UK, 1 in 2 people will be diagnosed with cancer at some point in their life. Genetic testing can help identify your risk of developing some of the most common types of cancer, so you can take action early.

of all cancers are linked to inherited genetic changes — including some of the most common gender-specific cancers like breast cancer and prostate cancer.

Genetic Counselling

A key part of your test is a 45-minute personalised session with one of our genetic counsellors. Genetics can be complex, but you're not alone—we're here to guide you through it. By exploring your family history, we can uncover valuable insights that could make a real difference to your health.

The Test

Our genetic cancer panel focuses on 50 carefully chosen genes, all backed by strong scientific evidence. While some tests look at more genes, many include ones with little clinical value. We focus on what’s most useful—so you get results you can actually act on.

The Lab

Research

Medicine is always evolving—and so are we. Our expert team stays up to date with the latest research and clinical guidelines, so you’re always getting advice that’s current, trusted, and tailored to you.

What's Next?

Genetic Counselling

Follow Up

Tailored Plan

Gene List

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How do you clone a Webflow Template?

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Cancer Risk Assessment Tool

Your Estimated Lifetime Cancer Risk

Ethnicity-Specific Risk Factors

General Population Risk Comparison

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Cancer
Genetic Testing