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APOA2
SNP Table
| variant | genotype | frequency | risk allele |
|---|---|---|---|
| rs189880241 | |||
| rs771259264 | |||
| rs11590967 | |||
| rs33941127 | |||
| rs11265564 | |||
| rs1346496201 | |||
| rs142522492 | |||
| rs2070901 | |||
| rs34448954 | |||
| rs4589131 | |||
| rs779695910 | |||
| rs10797094 | |||
| rs1136224 | |||
| rs11576415 | |||
| rs12094497 | |||
| rs2501876 | |||
| rs114305388 | |||
| rs11538340 | |||
| rs4233366 | |||
| rs3924264 |
Find on This Page
Summary
The APOA2 gene encodes apolipoprotein A2 [R].
APOA2 is part of HDL cholesterol metabolism. However, scientists aren’t sure of its specific function [R].
Mutations in APOA2 may cause high cholesterol [R].
Variants in this gene have also been linked to [R, R, R]:
- Autoimmune pancreatitis
- HDL cholesterol levels
- Weight gain from saturated fat
- Obesity
Protein names
Found in These Blog Articles
GHR Function
May stabilize HDL (high density lipoprotein) structure by its association with lipids, and affect the HDL metabolism.
More Information
From NCBI Gene: Familial hypercholesterolemia
From NCBI Gene: This gene encodes apolipoprotein (apo-) A-II, which is the second most abundant protein of the high density lipoprotein particles. The protein is found in plasma as a monomer, homodimer, or heterodimer with apolipoprotein D. Defects in this gene may result in apolipoprotein A-II deficiency or hypercholesterolemia. [provided by RefSeq, Jul 2008] From UniProt: May stabilize HDL (high density lipoprotein) structure by its association with lipids, and affect the HDL metabolism.
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