Overview

9:g.15304784C>A is a genetic variant associated with Cholecystitis and Cholelithiasis.

This variant is located on chromosome 9. The variations at position 15304784 are the genetic letters A/A, C/C, A/C

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 9:g.15304784C>A there are 3 currently known genotypes : A/A, C/C or A/C

Short Overview

Variant Location

9:g.15304784C>A is located on gene in chromsome 9. Use the genome browser to explore the location of 9:g.15304784C>A and its genetic neighbourhood.

Conditions & Traits

9:g.15304784C>A affects the following conditions and traits:

Pathogenicity

9:g.15304784C>A affects the following conditions:

Pharmacogenetics

9:g.15304784C>A affects the following drugs:

Diagnostics

9:g.15304784C>A 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 . Explore more variants and their effects on the body by browsing left and right along the DNA strand.

Loading Genome Browser...

Did you know genetic variants affect drugs?

Mutations are random changes in the DNA 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.

doctor_quote

Dr. Wallerstorfer

Conditions & Traits of 9:g.15304784C>A

The different genotypes of variant 9:g.15304784C>A can affect the expression or likelyhood of developing certain traits or conditions. Current research shows that 2 conditions and 0 traits are associated with 9:g.15304784C>A. The following table shows the relationship between genotypes and conditions and traits.

Did you know genetic variants affect drugs?

Genetic variants can influence how our body reacts to certain drugs. The presence of specific genetic variants can increase or decrease the efficiency and effectiveness of a drug, impacting how well it works inside our system. Additionally, certain genetic variants can heighten or lessen the toxicity of a drug, thereby affecting the risk of unwanted side effects. They can also alter how a drug is metabolized, which influences the appropriate dosage one should receive.

doctor_quote

Dr. Wallerstorfer

Variant Classification based on Scientific Studies

Scientific studies classifications aim to uncover how genetic variants function and their roles in diseases, traits, and evolution. Variants are categorized based on their functional impact, such as loss-of-function (reduces gene activity), gain-of-function (increases gene activity), neutral (no significant impact), or evolutionary conservation. This classification uses experimental data, population studies, and computational analyses to understand variant effects. Unlike clinical testing, which focuses on immediate health impacts, scientific studies explore broader genetic mechanisms and long-term implications.

Genotype

A

A

Level of evidence

doctor_quote

No Effect

Unisex

1 Sources

Participants: 641364

No available data

Genotype

A

C

Level of evidence

doctor_quote

No Effect

Unisex

1 Sources

Participants: 641364

No available data

Genotype

A

A

Level of evidence

doctor_quote

No Effect

Unisex

1 Sources

Participants: 641364

No available data

Genotype

A

C

Level of evidence

doctor_quote

No Effect

Unisex

1 Sources

Participants: 641364

No available data

Genotype

A

A

Level of evidence

doctor_quote

No Effect

Unisex

1 Sources

Participants: 665111

No available data

Genotype

A

C

Level of evidence

doctor_quote

No Effect

Unisex

1 Sources

Participants: 665111

No available data

Genotype

A

A

Level of evidence

doctor_quote

No Effect

Unisex

1 Sources

Participants: 665111

No available data

Genotype

A

C

Level of evidence

doctor_quote

No Effect

Unisex

1 Sources

Participants: 665111

No available data

Pharmacogenetics

The genetic variant 9:g.15304784C>A impacts how certain medications work in the body. This difference may cause some of us to require different dosage amounts to achieve the desired effects, while others might experience more apparent side-effects. As a result, healthcare providers may need to adjust prescriptions for those individuals with 9:g.15304784C>A. Ultimately, understanding our genetic makeup helps improve the overall effectiveness and usability of medications. Tailoring treatments based on genetics ensures a safer, more personalized healthcare experience.

Drugs related to 9:g.15304784C>A

All drugs that are linked to 9:g.15304784C>A are listed here.

Diagnostics

9:g.15304784C>A is commonly tested together with other variants on the same gene.

Related variants

Conditions and traits are often affected by more than one variant. It is important to understand these other factors to get a better understanding of how genetics affect certain conditions and traits. The following grid shows other variants that affect the same conditions and traits as 9:g.15304784C>A.

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 686030. 686030.

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

Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. (3/23/16)

Johannes Kettunen, Ayşe Demirkan, Peter Würtz, Harmen H M Draisma, Toomas Haller, Rajesh Rawal, Anika Vaarhorst, Antti J Kangas, Leo-Pekka Lyytikäinen, Matti Pirinen, René Pool, Antti-Pekka Sarin, Pasi Soininen, Taru Tukiainen, Qin Wang, Mika Tiainen, Tuulia Tynkkynen, Najaf Amin, Tanja Zeller, Marian Beekman, Joris Deelen, Ko Willems van Dijk, Tõnu Esko, Jouke-Jan Hottenga, Elisabeth M van Leeuwen, Terho Lehtimäki, Evelin Mihailov, Richard J Rose, Anton J M de Craen, Christian Gieger, Mika Kähönen, Markus Perola, Stefan Blankenberg, Markku J Savolainen, Aswin Verhoeven, Jorma Viikari, Gonneke Willemsen, Dorret I Boomsma, Cornelia M van Duijn, Johan Eriksson, Antti Jula, Marjo-Riitta Järvelin, Jaakko Kaprio, Andres Metspalu, Olli Raitakari, Veikko Salomaa, P Eline Slagboom, Melanie Waldenberger, Samuli Ripatti, Mika Ala-Korpela

PubMed: 27005778
Genome-wide association study of serum coenzyme Q10 levels identifies susceptibility loci linked to neuronal diseases. (7/1/16)

Frauke Degenhardt, Petra Niklowitz, Silke Szymczak, Gunnar Jacobs, Wolfgang Lieb, Thomas Menke, Matthias Laudes, Tõnu Esko, Stephan Weidinger, Andre Franke, Frank Döring, Simone Onur

PubMed: 27149984
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