Overview
rs628031 is a genetic variant on gene SLC22A1.
This variant is located on chromosome 6. The variations at position 160139813 are the genetic letters A/A, G/G, A/G
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 rs628031 there are 3 currently known genotypes : A/A, G/G or A/G
Short Overview
Variant Location
rs628031 is located on gene SLC22A1 in chromsome 6. Use the genome browser to explore the location of rs628031 and its genetic neighbourhood.
Conditions & Traits
rs628031 affects the following conditions and traits:
There are currently 0 conditions and 0 traits associated with rs628031.
Pathogenicity
rs628031 affects the following conditions:
There are currently 0 conditions associated with rs628031.
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 on gene SLC22A1. Explore more variants and their effects on the body by browsing left and right along the DNA strand.
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.
Conditions & Traits of rs628031
Current research shows 0 conditions and 0 traits.
Conditions
0Pharmacogenetics
The genetic variant rs628031 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 rs628031. 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.
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more info
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more info
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Genotype
Impacts
Breakdown
Drug Effect
Side Effects
Dosage
Summary
No summary available.
Level of evidence
More info
Genotype
Impacts
Breakdown
Drug Effect
Side Effects
Dosage
Summary
No summary available.
Level of evidence
More info
Genotype
Impacts
Breakdown
Drug Effect
Side Effects
Dosage
Summary
No summary available.
Level of evidence
More info
Legend:
Increased
Decreased
No known effect
Drugs related to rs628031
All drugs that are linked to rs628031 are listed here.
Studies and Sources
All of the resources below examine variant rs628031
Aliya A. Rizvi, Mohammad Abbas, Sushma Verma, Shrikant Verma, Almas Khan, Syed T. Raza, Farzana Mahdi
Elizabeth Paz-Pacheco, Jose B Nevado, Eva Maria C Cutiongco-de la Paz, Gabriel V Jasul, Aimee Yvonne Criselle L Aman, Elizabeth Laurize A Ribaya, Mark David G Francisco, Ma Luz Vicenta V Guanzon, May L Uyking-Naranjo, Ma Cecille S Añonuevo-Cruz, Maria Patricia Deanna D Maningat, Cristina V Jaring, Paulette D Nacpil-Dominguez, Aniza B Pala-Mohamad, Abigail U Canto, John Paul M Quisumbing, Annabelle Marie M Lat, Diane Carla C Bernardo, Noemie Marie M Mansibang, Karell Jo Angelique C Calpito, Vincent Sean D Ribaya, Julius Patrick Y Ferrer, Jessica H Biwang, Jodelyn B Melegrito, Christian Deo T Deguit, Carlos Emmanuel G Panerio
Adiel Ortega-Ayala, Nidia Samara Rodríguez-Rivera, Fernando de Andrés, Adrián LLerena, Eliseo Pérez-Silva, Adriana Guadalupe Espinosa-Sánchez, Juan Arcadio Molina-Guarneros