23andMe Personal Genome Service (PGS) Genetic Health Risk Test for Hereditary Thrombophilia vs Invitae Genetic Testing

Similar category, different focus. These tools serve overlapping but distinct needs. Comparability 65/100 Comparability is an AI-graded 0–100 score of how directly these two tools compete — higher means a more apples-to-apples comparison.

AI Verdict

23andMe's tool is a direct-to-consumer genetic test specifically for hereditary thrombophilia, focusing on two common genetic variants. Invitae, now part of Labcorp, offers a much broader range of comprehensive genetic testing services across numerous medical specialties, utilizing AI for interpretation and providing genetic counseling. While both offer genetic testing, 23andMe is a specialized direct-to-consumer screening tool, whereas Invitae provides extensive, medically-focused diagnostic and screening services often integrated with healthcare providers.

Choose 23andMe Personal Genome Service (PGS) Genetic Health Risk Test for Hereditary Thrombophilia if…

Choose 23andMe Personal Genome Service (PGS) Genetic Health Risk Test for Hereditary Thrombophilia if you are primarily interested in a direct-to-consumer screening for specific genetic variants (Factor V Leiden and Prothrombin G20210A) associated with an increased risk of developing harmful blood clots. This test is particularly relevant for individuals of European descent seeking personal genetic insights for proactive health discussions, and it includes ancestry reports.

View 23andMe Personal Genome Service (PGS) Genetic Health Risk Test for Hereditary Thrombophilia →

Choose Invitae Genetic Testing if…

Choose Invitae Genetic Testing if you require comprehensive genetic testing across various medical specialties, especially when seeking a diagnosis for hereditary conditions or guiding personalized patient care. Invitae offers extensive test catalogs for conditions like hereditary cancers and pediatric disorders, includes genetic counseling services, and provides flexible billing options with most tests covered by health plans.

View Invitae Genetic Testing →

Reviewed by Pouyan Golshani, MD — Interventional Radiologist

Quick Comparison

Feature 23andMe Personal Genome Service (PGS) Genetic Health Risk Test for Hereditary Thrombophilia Invitae Genetic Testing
Pricing $199 1
Deployment Cloud-based (for data access and reports), At-home kit (for sample collection) Cloud-based
BAA Available No AI-estimated Unknown
FDA Status 1 AI-estimated 1 AI-estimated
HIPAA No AI-estimated Unknown

Head-to-Head

AI-generated assessment across six dimensions based on each tool's documented features and compliance posture. Grounded in public data — not a substitute for hands-on evaluation.

Usability

23andMe Personal Genome Service (PGS) Genetic Health Risk Test for Hereditary Thrombophilia

23andMe offers a direct-to-consumer model with an at-home saliva collection kit, making it highly accessible and convenient for users. Invitae, while offering an online portal for ordering and viewing reports, generally requires a healthcare provider to order tests, which adds a step to the user journey.

Clinical Value

Invitae Genetic Testing

Invitae provides comprehensive genetic testing across many medical specialties with AI-powered interpretation and includes genetic counseling services, offering a broader and deeper clinical utility. 23andMe's Hereditary Thrombophilia test focuses on two specific genetic variants and is primarily for personal genetic insights to inform discussions with healthcare professionals, rather than comprehensive diagnostic testing. Invitae's tests have also been validated with high sensitivity and specificity for detecting deletions and duplications in genes across various conditions.

Pricing & Value

Invitae Genetic Testing

Invitae offers flexible billing options, including insurance coverage for most tests, with typical patient out-of-pocket costs ranging from $0-$100, and a pre-pay option of $250 per clinical area. They also have financial assistance programs and sponsored no-charge testing for eligible patients. 23andMe's specific Hereditary Thrombophilia test is part of their Health + Ancestry Service priced at $199, and is generally not covered by insurance.

Enterprise Readiness

Invitae Genetic Testing

Invitae is part of Labcorp, indicating a strong enterprise infrastructure and broad reach through Labcorp's nationwide patient service centers. They are HIPAA compliant and offer a Business Associate Agreement (BAA), which are crucial for enterprise healthcare integrations. 23andMe does not offer a BAA and is not HIPAA compliant, limiting its readiness for direct enterprise healthcare system integration.

Innovation

Invitae Genetic Testing

Invitae leverages AI-powered interpretation for variant classification and offers comprehensive multi-gene panel testing, including RNA analysis to supplement DNA results, which can provide more definitive results for complex cases. 23andMe's innovation lies in its direct-to-consumer model and FDA clearance for specific genetic health risk reports, but its testing for hereditary thrombophilia focuses on a limited number of common variants.

Support & Docs

Invitae Genetic Testing

Invitae provides extensive support, including genetic counseling services at no additional cost in the US, US territories, and Canada, as well as dedicated client services and clinical practice resources for healthcare providers. 23andMe offers educational resources and customer care, but explicitly states that its screening does not include genetic counseling.

Feature-by-Feature

Detail beyond the Quick Comparison summary. For pricing, deployment, BAA, FDA, and HIPAA see the Overview tab.

Feature 23andMe Personal Genome Service (PGS) Genetic Health Risk Test for Hereditary Thrombophilia Invitae Genetic Testing
Tool Name 23andMe Personal Genome Service (PGS) Genetic Health Risk Test for Hereditary Thrombophilia Invitae Genetic Testing
Company 23andMe Invitae (now part of Labcorp)
Primary Focus Detection of specific genetic variants (Factor V Leiden and Prothrombin G20210A) associated with hereditary thrombophilia risk Comprehensive genetic testing services across many medical specialties for diagnosis of hereditary conditions
Key Features Detection of Factor V Leiden and Prothrombin G20210A variants, direct-to-consumer saliva sample collection, personalized online genetic health risk reports, ancestry reports, educational resources Comprehensive genetic testing across many medical specialties, AI-powered interpretation, genetic counseling services included, flexible billing, access to Labcorp patient service centers, online portal, Family History Tool

Videos

Demos, reviews, and walkthroughs featuring 23andMe Personal Genome Service (PGS) Genetic Health Risk Test for Hereditary Thrombophilia and Invitae Genetic Testing.

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Frequently Asked Questions

Invitae is designed for integration into clinical workflows, offering an online portal for ordering, tracking, and viewing patient reports, and actively working on EHR integrations to streamline the process for healthcare providers. 23andMe, being a direct-to-consumer test, requires patients to collect their own saliva samples at home, and physicians would primarily engage with the personalized online genetic health risk reports provided to the patient.
Invitae offers significant EHR integration capabilities, including an agreement to provide access to its genetic test results directly through Epic's Aura specialty diagnostics suite, aiming to incorporate results into standard workflows and reduce administrative burdens. 23andMe, as a direct-to-consumer service, does not offer direct EHR integration; physicians would receive patient-initiated reports.
Invitae's next-generation sequencing multi-gene panels have demonstrated over 99.9% analytic sensitivity and specificity for detecting sequence alterations and intragenic deletions/duplications, with validation studies showing greater than 99% accuracy across various variant types. 23andMe's Hereditary Thrombophilia test also shows high accuracy, with method comparison studies demonstrating over 99% agreement with sequencing results for the specific Factor V Leiden and Prothrombin G20210A variants it detects.
Invitae offers comprehensive genetic testing across many medical specialties, including maternal-fetal medicine, oncology, and pediatrics, with broad test offerings informing every stage of life. 23andMe's Hereditary Thrombophilia test is specifically indicated for hematology and laboratory medicine, focusing on two common genetic variants associated with an increased risk of developing harmful blood clots, primarily relevant for people of European descent.
Invitae provides extensive support, including board-certified genetic counselors available to assist clinicians with case reviews, test selection, result interpretation, and post-test counseling for patients. 23andMe offers educational resources for healthcare professionals and encourages consultation with a healthcare professional or genetic counselor for any concerns about results.
Invitae is committed to transparency in data use, submitting clinically reported variants and their classifications to ClinVar in compliance with HIPAA, and allowing patients to set preferences for how their de-identified data is used for research. 23andMe provides personalized online genetic health risk reports to the individual, and while it emphasizes privacy, specific audit-trail features for physician review beyond the patient's report are not detailed.
Invitae, now part of Labcorp, has completed over 400 customer EHR integrations and has a dedicated Epic-certified EHR integration team, suggesting robust capabilities for multi-site rollout and scalability within healthcare systems. 23andMe, as a direct-to-consumer model, focuses on individual at-home sample collection and online report access, which inherently scales to individual users but does not offer specific features for multi-site healthcare system integration.

Backers

Who funded each tool's parent company.

23andMe Personal Genome Service (PGS) Genetic Health Risk Test for Hereditary Thrombophilia

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