Standard
Asparaginase-induced acute pancreatitis in acute lymphoblastic leukemia (onset time)
CPA2 · rs199695765
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 with typical/baseline likelihood of Asparaginase-induced acute pancreatitis in acute lymphoblastic leukemia (onset time) — no copies of the reported risk allele. (GWAS Catalog, J Clin Oncol 2016, PMID:27114598)
C/T
Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Asparaginase-induced acute pancreatitis in acute lymphoblastic leukemia (onset time). (GWAS Catalog, J Clin Oncol 2016, PMID:27114598)
T/T
Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Asparaginase-induced acute pancreatitis in acute lymphoblastic leukemia (onset time) compared to the general population. (GWAS Catalog, J Clin Oncol 2016, PMID:27114598)
Source: GWAS Catalog, J Clin Oncol 2016, PMID:27114598
Questions about rs199695765
What is rs199695765?
rs199695765 is a single position in the genome, in or near the CPA2 gene. Published research associates it with asparaginase-induced acute pancreatitis in acute lymphoblastic leukemia (onset time). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs199695765 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 rs199695765 come from?
GWAS Catalog, J Clin Oncol 2016, PMID:27114598. 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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