rs368001205: what the research says
A sex-specific genetic locus on chromosome 11 associated with chronic pain in females.
What each genotype means
Typical genetic profile
This genotype represents the most common form of this genetic locus. Research into this variant is limited, and there is no established evidence that this specific combination influences chronic pain susceptibility.
This is the most frequent genotype observed across global populations.
Rare variant carrier
You carry one copy of the minor allele associated with this locus. Because the evidence linking this variant to chronic pain in females is limited, it is unclear if this genotype has any functional impact on your health.
This genotype is rare and observed at very low frequencies in most populations.
Rare variant carrier
You carry two copies of the minor allele at this locus. While this variant has been cataloged as a potential sex-specific genetic marker for chronic pain in females, the current evidence is limited and not sufficient to draw clinical conclusions about your personal risk.
This genotype is extremely rare across all studied ancestral groups.
Rare
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