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ANKRD65 rs758603246: what the research says

rs758603246
Trait
Moderate evidenceGene: ANKRD65

A rare variant in the 5'-UTR of ANKRD65 that appears in linkage disequilibrium with specific ancestral haplotypes.

What each genotype means

A/ALower attention

Common ancestral genotype

This is the most common genotype observed in the general population. It does not carry the rare variant associated with specific ancestral haplotypes linked to the ANKRD65 gene region.

This is the predominant genotype found across all major global populations.

A/GModerate attention

Rare variant carrier

You carry one copy of this rare variant located in the 5'-UTR of the ANKRD65 gene. Research indicates this variant is often found in linkage disequilibrium with other specific genetic markers, meaning it is frequently inherited alongside other nearby variations on the same chromosome.

This genotype is rare and typically observed only within specific ancestral groups where the associated haplotype is present.

G/GModerate attention

Rare homozygous variant

You carry two copies of this rare variant in the 5'-UTR of the ANKRD65 gene. Because this variant is linked to specific ancestral haplotypes, its presence in a homozygous state suggests inheritance of this specific genetic background from both parents.

This genotype is extremely rare and is only found in populations where the specific ancestral haplotype is prevalent.

Rare

Our full long-form research profile for rs758603246 — genotype interpretations, evidence review, and FAQ — is being written and will appear on this page soon.

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