rs3197999 is a genetic variant on gene MST1.
This variant is located on chromosome 3. The variations at position 49684099 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 rs3197999 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
rs3197999 is located on gene MST1 in chromsome 3. Use the genome browser to explore the location of rs3197999 and its genetic neighbourhood.
rs3197999 affects the following conditions and traits:
There are currently 0 conditions and 0 traits associated with rs3197999.
rs3197999 affects the following conditions:
There are currently 0 conditions associated with rs3197999.
We do not have any data that links rs3197999 to any drugs.
rs3197999 is commonly tested together with other variants on the same gene.
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 MST1. Explore more variants and their effects on the body by browsing left and right along the DNA strand.
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
Current research shows 0 conditions and 0 traits.
rs3197999 is commonly tested together with other variants on the same gene.
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 3197999. 3197999.
All of the resources below examine variant rs3197999
William K.K. Wu, Rui Sun, Tao Zuo, Yuanyuan Tian, Zhirong Zeng, Jeffery Ho, Justin C.Y. Wu, Francis K.L. Chan, Matthew T.V. Chan, Jun Yu, Joseph J.Y. Sung, Sunny H. Wong, Maggie H. Wang, Siew C. Ng
Veronika Fedirko, Hannah B. Mandle, Wanzhe Zhu, David J. Hughes, Afshan Siddiq, Pietro Ferrari, Isabelle Romieu, Elio Riboli, Bas Bueno-de-Mesquita, Fränzel J.B. van Duijnhoven, Peter D. Siersema, Anne Tjønneland, Anja Olsen, Vittorio Perduca, Franck Carbonnel, Marie-Christine Boutron-Ruault, Tilman Kühn, Theron Johnson, Aleksandrova Krasimira, Antonia Trichopoulou, Periklis Makrythanasis, Dimitris Thanos, Salvatore Panico, Vittorio Krogh, Carlotta Sacerdote, Guri Skeie, Elisabete Weiderpass, Sandra Colorado-Yohar, Núria Sala, Aurelio Barricarte, Maria-Jose Sanchez, Ramón Quirós, Pilar Amiano, Björn Gylling, Sophia Harlid, Aurora Perez-Cornago, Alicia K. Heath, Konstantinos K. Tsilidis, Dagfinn Aune, Heinz Freisling, Neil Murphy, Marc J. Gunter, Mazda Jenab
Jingjing Zhu, Xiang Shu, Xingyi Guo, Duo Liu, Jiandong Bao, Roger L Milne, Graham G Giles, Chong Wu, Mengmeng Du, Emily White, Harvey A Risch, Nuria Malats, Eric J. Duell, Phyllis J. Goodman, Donghui Li, Paige Bracci, Verena Katzke, Rachel E Neale, Steven Gallinger, Stephen K Van Den Eeden, Alan A Arslan, Federico Canzian, Charles Kooperberg, Laura E Beane-Freeman, Ghislaine Scelo, Kala Visvanathan, Christopher A. Haiman, Loïc Le Marchand, Herbert Yu, Gloria M Petersen, Rachael Stolzenberg-Solomon, Alison P Klein, Qiuyin Cai, Jirong Long, Xiao-Ou Shu, Wei Zheng, Lang Wu