23andMe – Official Site

Posted: November 9, 2017 at 1:47 pm

DNA Genetic Testing & Analysis – 23andMe

23 pairs of chromosomes. One unique you.

*when you buy 2+ Ancestry Service kits

savings based on regular price per kit

Buy 2 or more kits and celebrate your family’s genetic connections.

savings based on regular price per kit

Experience your ancestry in a new way! Get a breakdown of your global ancestryby percentages, connect with DNA relatives and more.learn more

Learn how your genetics can influence your risk for certain diseases and how your genes play a role in yourwell-being and lifestyle choices.

Get an even more comprehensive understanding of your genetics. Receive75+ online reports on your ancestry, traits and health – and more.learn more

*One kit for $69. Savings based on regular price per kit.

We hear from thousands of customers around the world who write in to tell us abouttheir 23andMe experienceand the impact it has had on their life.

See stories that inspire us.

You are made of cells. And the cells in your body have 23 pairs of chromosomes. Yourchromosomes are made of DNA, which can tell you a lot about you. Explore your 23 pairstoday.

Find out what your 23 pairs of chromosomes can tell you.

Your DNA analysis is performed in US laboratories that are certified to meet CLIAstandardsthe Clinical Laboratory Improvement Amendments of 1988.

A CLIA-certified lab must meet certain quality standards, including qualificationsfor individuals who perform the test and other standards that ensure the accuracyand reliability of results.

We use leading technology to genotype your DNAa custom Illumina HumanOmniExpress-24format chip.

Learn more about our process.

Provide your saliva sample from home. Mail it back to our lab in the same kit itcame inthe postage is pre-paid.

We bring your genetics to you.

Learn more about how it works.

23andMe was founded in 2006 to help people access, understand and benefitfrom the human genome.

We have more than two million genotyped customers around the world.

In 2015, 23andMe was granted authorization by the US Food and DrugAdministration (FDA) to market the first direct-to-consumer genetic test.

23andMe offers two Personal Genetic Services: Health + Ancestry and Ancestry. Both services require submittinga saliva sample using our saliva collection kit that you send to the lab for analysis.

Our Health + Ancestry Service provides insights on your genetic health risks*, carrier status*, traits,wellness and ancestry. We analyze, compile and distill the information extracted from yourDNA into 75+ reports you can access online and share with family and friends.See full list of reports offered.

Our Ancestry Service helps you understand who you are, where your DNA comes from and your family story. Weanalyze, compile and distill your DNA information into reports on your Ancestry Composition,Maternal & Paternal Haplogroups, NeanderthalAncestry, Your DNA Family and provide a DNA Relatives tool to enable you to connect with relatives who sharesimilar DNA.

*The 23andMe PGS test uses qualitative genotyping to detect clinically relevant variants in the genomic DNA of adultsfrom saliva collected using an FDA-cleared collection device (OrageneDX model OGD-500.001) for the purpose ofreporting and interpreting genetic health risks and reporting carrier status. It is not intended to diagnose anydisease. The relevance of each report may vary based on ethnicity. Each genetic health risk report describes if aperson has variants associated with a higher risk of developing a disease, but does not describe a person’s overallrisk of developing the disease. These reports are not intended to tell you anything about your current state ofhealth, or to be used to make medical decisions, including whether or not you should take a medication or how much ofa medication you should take. Our carrier status reports can be used to determine carrier status, but cannotdetermine if you have two copies of any genetic variant. These carrier reports are not intended to tell you anythingabout your risk for developing a disease in the future or anything about the health of your fetus, or your newbornchild’s risk of developing a particular disease later in life. For Gaucher Disease Type 1, we provide a single reportthat includes information on both carrier status and genetic health risk.The Parkinson’s Disease genetic health risk report (i) is indicated for reporting of the G2019S variant in the LRRK2gene, and the N370S variant in the GBA gene, (ii) describes if a person has variants associated with an increased riskof developing Parkinson’s disease, and (iii) is most relevant for people of European, Ashkenazi Jewish, and NorthAfrican Berber descent.

$99

$49*

AncestryService

Get a breakdown of your global ancestry, connect with DNA relatives and more.

$199

HealthService

Learn how your genetics can influence your risk for certain diseases.

$199

Health +Ancestry Service

Receive 75+ online reports on your ancestry, traits and health -and more.

*When you buy 2+ kits. One kit for $69.Savings based on regular price per kit.

2 variantsinthe ARMS2 and CFH genes;relevant for European descent

2 variantsinthe SERPINA1 gene;relevant for European descent

2 variantsnearthe HLA-DQA1 and HLA-DQB1 genes;relevant for European descent

2 variantsinthe HFE gene;relevant for European descent

2 variantsinthe F2 and F5 genes;relevant for European descent

1 variantinthe APOE gene;variant found and studied in many ethnicities

2 variantsinthe LRRK2 and GBA genes;relevant for European, Ashkenazi Jewish, North African Berber descent

1 variant in the SACSgene; relevant for French Canadian descent

1 variant in the SLC12A6gene; relevant for French Canadian descent

3 variants in the PKHD1gene

10 variants in the HBBgene; relevant for Cypriot, Greek, Italian, Sardinian descent

1 variant in the BLMgene; relevant for Ashkenazi Jewish descent

3 variants in the ASPAgene; relevant for Ashkenazi Jewish descent

2 variants in the PMM2gene; relevant for Danish descent

28 variants in the CFTRgene; relevant for European, Hispanic/Latino, Ashkenazi Jewish descent

2 variants in the HSD17B4gene

1 variant in the DLDgene; relevant for Ashkenazi Jewish descent

1 variant in the IKBKAPgene; relevant for Ashkenazi Jewish descent

3 variants in the FANCCgene; relevant for Ashkenazi Jewish descent

1 variant in the BCS1Lgene; relevant for Finnish descent

3 variants in the GBAgene; relevant for Ashkenazi Jewish descent

1 variant in the G6PCgene; relevant for Ashkenazi Jewish descent

2 variants in the SLC37A4gene

3 variants in the ALDOBgene; relevant for European descent

3 variants in the LAMB3gene

1 variant in the LRPPRCgene; relevant for French Canadian descent

1 variant in the SGCAgene; relevant for Finnish descent

1 variant in the SGCBgene; relevant for Southern Indiana Amish descent

1 variant in the FKRPgene; relevant for European descent

3 variants in the ACADMgene; relevant for Northern European descent

2 variants in the BCKDHBgene; relevant for Ashkenazi Jewish descent

1 variant in the MCOLN1gene; relevant for Ashkenazi Jewish descent

1 variant in the CLN5gene; relevant for Finnish descent

3 variants in the PPT1gene; relevant for Finnish descent

3 variants in the SMPD1gene; relevant for Ashkenazi Jewish descent

1 variant in the NBNgene; relevant for Eastern European descent

2 variants in the GJB2gene; relevant for Ashkenazi Jewish, European descent

6 variants in the SLC26A4gene

23 variants in the PAHgene; relevant for Northern European descent

1 variant in the GRHPRgene; relevant for European descent

1 variant in the PEX7gene

1 variant in the SLC17A5gene; relevant for Finnish, Swedish descent

1 variant in the HBBgene; relevant for African descent

1 variant in the ALDH3A2gene; relevant for Swedish descent

4 variants in the HEXAgene; relevant for Ashkenazi Jewish, Cajun descent

4 variants in the FAHgene; relevant for French Canadian, Finnish descent

1 variant in the PCDH15gene; relevant for Ashkenazi Jewish descent

1 variant in the CLRN1gene; relevant for Ashkenazi Jewish descent

1 variant in the PEX1gene

when you buy 2+ Ancestry Service kits,savings based on regular price per kit

Health + Ancestry $199

2 variantsinthe ARMS2 and CFH genes;relevant for European descent

2 variantsinthe SERPINA1 gene;relevant for European descent

2 variantsnearthe HLA-DQA1 and HLA-DQB1 genes;relevant for European descent

2 variantsinthe HFE gene;relevant for European descent

2 variantsinthe F2 and F5 genes;relevant for European descent

1 variantinthe APOE gene;variant found and studied in many ethnicities

2 variantsinthe LRRK2 and GBA genes;relevant for European, Ashkenazi Jewish, North African Berber descent

1 variant in the SACSgene; relevant for French Canadian descent

1 variant in the SLC12A6gene; relevant for French Canadian descent

More here:
23andMe – Official Site

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