HLA-A rs1136903: what the research says
This variant is a well-established polymorphism located within the HLA-A gene region.
What each genotype means
Common HLA-A variant
This genotype represents one of the common configurations for this HLA-A region variant. Research indicates this is a well-established polymorphism, though specific clinical implications for individuals remain limited and are not diagnostic of any condition.
This genotype is observed frequently across diverse global populations.
Common HLA-A variant
This genotype represents a heterozygous configuration for this HLA-A region variant. As this is a common polymorphism, it is generally considered a normal variation in the human genome without specific clinical diagnostic significance.
This genotype is found in a significant portion of the population across various ancestries.
Common HLA-A variant
This genotype represents the alternative homozygous configuration for this HLA-A region variant. Current scientific literature identifies this as a common polymorphism, and it does not serve as a standalone indicator for health outcomes or medical conditions.
This genotype is common and widely distributed across global populations.
0.3246
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