Overview

rs368187 is a genetic variant.

This variant is located on chromosome 14. The variations at position 36063370 are the genetic letters A/A, C/C, G/G, T/T, A/C, C/G, G/T, A/T, A/G, C/T

Since humans have each twice (one from each parent), these letter-variations occur on both chromosomes. People can have the same or different letters on both chromosomes. Every person's individual variation combination is referred to as genotype. For variant rs368187 there are 10 currently known genotypes : A/A, C/C, G/G, T/T, A/C, C/G, G/T, A/T, A/G or C/T

Short Overview

Variant Location

rs368187 is located on gene in chromsome 14. Use the genome browser to explore the location of rs368187 and its genetic neighbourhood.

Conditions & Traits

rs368187 affects the following conditions and traits:

There are currently 0 conditions and 0 traits associated with rs368187.

Pathogenicity

rs368187 affects the following conditions:

There are currently 0 conditions associated with rs368187.

Pharmacogenetics

We do not have any data that links rs368187 to any drugs.

Diagnostics

rs368187 is commonly tested together with other variants on the same gene.

Genome Browser

This interactive browser visualizes what no human can see with the naked eye - our DNA. From a down to a specific position on a . The position you are looking at here is the exact location of variant rs. Explore more variants and their effects on the body by browsing left and right along the DNA strand.

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Did you know genetic variants affect drugs?

Mutations are changes in genes and genetic variations are differences in the DNA among people. Variants are tiny changes in just one piece of the DNA while haplotypes are groups of these changes that usually come together.

Dr. Wallerstorfer

Conditions & Traits of rs368187

Current research shows 0 conditions and 0 traits.

Diagnostics

rs368187 is commonly tested together with other variants on the same gene.

Genotype Distribution

Knowing your genome can actually tell you a lot about your ancestors.

The prevalence of the different genotypes is based on the native inhabitants of a region. In the map below you see how common each genotype is in the native inhabitants of those regions. Since genetic material is passed down form generation to generation, your DNA shows traces of the geographical origins of your ancestors.

This data is based on “The 1000 Genomes Project” which established one of the most detailed overviews of human genetic variations across the globe. The regions are broadly categorized into five continental groups: Africa, America, Europe, South Asia and East Asia. All continental groups together display the global prevalence. Click through the regions, to learn more about the local prevalence of the possible genotypes.

At present, there is no distribution data available for SNP 368187. 368187.

The Genotype Distribution in the selected area is:
Legend:
Included regions
Excluded regions
no-data

Studies and Sources

All of the resources below examine variant rs368187

Fine mapping of 14q13 reveals novel variants associated with different histological subtypes of papillary thyroid carcinoma (10/30/18)

Jaroslaw Jendrzejewski, Sandya Liyanarachchi, Andrew Eiterman, Andrew Thomas, Huiling He, Rebecca Nagy, Leigha Senter, Krzysztof Sworczak, Albert de la Chapelle

PMC: 6294684
Genetic Mutations and Variants in the Susceptibility of Familial Non-Medullary Thyroid Cancer (11/18/20)

Fabíola Yukiko Miasaki, Cesar Seigi Fuziwara, Gisah Amaral de Carvalho, Edna Teruko Kimura

PMC: 7698903
Emerging Biomarkers in Thyroid Practice and Research (12/31/21)

Shipra Agarwal, Andrey Bychkov, Chan-Kwon Jung

PMC: 8744846
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