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ADAMTS13 activity

ADAMTS13 · rs3118667

Stands on its own. Nothing else here links to this position yet — but the page above is the point: what the research found, what each genotype means, and where it came from, in language you can read. Links to conditions, drugs and the senses appear automatically if we write them.

What each result means

C/C Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of ADAMTS13 activity compared to the general population.

C/T Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with ADAMTS13 activity.

T/T Published research associates this genotype with typical/baseline likelihood of ADAMTS13 activity — no copies of the reported risk allele.

Source

Genetic variants in the ADAMTS13 and SUPT3H genes are associated with ADAMTS13 activity

de Vries PS, Boender J, Sonneveld MA, Rivadeneira F, Ikram MA, Rottensteiner H, Hofman A, Uitterlinden AG, Leebeek FW, Franco OH, Dehghan A, de Maat MP

Blood · 2015 · PMID 25934476

Questions about rs3118667

What is rs3118667?

rs3118667 is a single position in the genome, in or near the ADAMTS13 gene. Published research associates it with adamts13 activity. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs3118667 mean I will get this?

No. Common variants like this one move a probability slightly and, on their own, rarely decide anything about one person. Nothing on this page is a diagnosis, and health decisions should be made with a clinician who can see your whole picture.

Where does the information about rs3118667 come from?

GWAS Catalog, Blood 2015, PMID:25934476. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

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