Upload the DNA data file of the test

23andMe, AncestryDNA, FamilyTreeDNA, MyHeritage

and get an enhanced
personalized health report
free without registration

Files accepted .txt, .csv, .zip, .csv.gz

File data is not stored on the server

SNP information rs3761863

RS3761863

Normal allele: AA

Missense LRRK2 variant is a risk factor for Parkinson's disease.

Polymorphism rs3761863 is related to topics like this:

Parkinson is a genetic disease

A disorder that progresses gradually within the nervous system is known as Parkinson's disease. It...

Research and publications:

  16960813   LRRK2 G2019S in families with Parkinson disease who originated from Europe and the Middle East: evidence of two distinct founding events beginning two millennia ago.

  17614198   Lrrk2 mutations in South America: the Chilean Parkinson's disease study.

  18952485   Haplotype analysis of Lrrk2 R1441H carriers with parkinsonism.

  20301387   LRRK2 Parkinson Disease.

  20669299   LRRK2 variation and Parkinson's disease in African Americans.

  21885347   Association of LRRK2 exonic variants with Parkinson's disease susceptibility: a case-control study.

  26844546   A Missense LRRK2 Variant Is a Risk Factor for Excessive Inflammatory Responses in Leprosy.

  32433683   Association of NOD2 and IFNG single nucleotide polymorphisms with leprosy in the Amazon ethnic admixed population.

Is multiple sclerosis hereditary disease

The presence of lesions on the brain and spinal cord is indicative of multiple sclerosis, a...

Dementia is genetic

Dementia is characterized as a syndrome, rather than a singular disease. Individuals with early...

Alzheimer's disease is hereditary

Alzheimer's disease is a degenerative brain disease that causes dementia, resulting in a gradual...

List of all diseases
en
|
de
|
fr
|
es
|
it
|
ua
|
ru

About

Documents

Support