Note: This variant has not been sufficiently evaluated by a GET-Evidence editor.
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You are viewing an old version of this page that was saved on January 7, 2010 at 6:45am by Alexander Wait Zaranek.
Insufficiently evaluated pathogenic
(The "insufficiently evaluated" qualifier is assigned automatically based on the above evidence and importance scores.)
Summary of published research, and additional commentary
Added in this revision:
Cenarro A, Artieda M, Castillo S, Mozas P, Reyes G, Tejedor D, Alonso R, Mata
P, Pocoví M, Civeira F; Spanish FH group. A common variant in the ABCA1 gene is
associated with a lower risk for premature coronary heart disease in familial
hypercholesterolaemia. J Med Genet. 2003 Mar;40(3):163-8. PubMed PMID: 12624133;
PubMed Central PMCID: PMC1735389.
Katzov H, Bennet AM, Höglund K, Wiman B, Lütjohann D, Brookes AJ, Andreasen N,
Blennow K, De Faire U, Prince JA. Quantitative trait loci in ABCA1 modify
cerebrospinal fluid amyloid-beta 1-42 and plasma apolipoprotein levels. J Hum
Genet. 2006;51(3):171-9. Epub 2005 Dec 22. PubMed PMID: 16372134.