Standard

Chronic lymphocytic leukemia

SCN3B · rs35923643

Where this position leads

Condition: Chronic Lymphocytic Leukaemia

rs35923643 Condition: Chronic Lymphocytic Leukaemia Chronic Lymphocytic Leukaemia Condition rs35923643 rs35923643 SCN3B

What each result means

A/A Published research associates this genotype with typical/baseline likelihood of Chronic lymphocytic leukemia — no copies of the reported risk allele.
A/G Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Chronic lymphocytic leukemia.
G/G Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Chronic lymphocytic leukemia compared to the general population.
Source

Questions about rs35923643

What is rs35923643?

rs35923643 is a single position in the genome, in or near the SCN3B gene. Published research associates it with chronic lymphocytic leukemia. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs35923643 linked to?

On MyGeneLog this position is linked to Chronic Lymphocytic Leukaemia. The research behind each link, and its sources, are set out on that condition page.

Does having rs35923643 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 rs35923643 come from?

GWAS Catalog, Nat Commun 2017, PMID:28165464. 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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