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Immunoglobulin light chain (AL) amyloidosis

SMARCD3 · rs79419269

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 Immunoglobulin light chain (AL) amyloidosis compared to the general population. (GWAS Catalog, Leukemia 2016, PMID:28025584)

C/T Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Immunoglobulin light chain (AL) amyloidosis. (GWAS Catalog, Leukemia 2016, PMID:28025584)

T/T Published research associates this genotype with typical/baseline likelihood of Immunoglobulin light chain (AL) amyloidosis — no copies of the reported risk allele. (GWAS Catalog, Leukemia 2016, PMID:28025584)

Source: GWAS Catalog, Leukemia 2016, PMID:28025584

Questions about rs79419269

What is rs79419269?

rs79419269 is a single position in the genome, in or near the SMARCD3 gene. Published research associates it with immunoglobulin light chain (al) amyloidosis. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs79419269 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 rs79419269 come from?

GWAS Catalog, Leukemia 2016, PMID:28025584. 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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