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rs2066715

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs2066715(A;A)
Make rs2066715(A;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position104825752
GeneABCA1
is asnp
is mentioned by
dbSNPrs2066715
ebirs2066715
HLIrs2066715
Exacrs2066715
Varsomers2066715
Maprs2066715
PheGenIrs2066715
hapmaprs2066715
1000 genomesrs2066715
hgdprs2066715
ensemblrs2066715
gopubmedrs2066715
geneviewrs2066715
scholarrs2066715
googlers2066715
pharmgkbrs2066715
gwascentralrs2066715
openSNPrs2066715
23andMers2066715
23andMe allrs2066715
SNP Nexus

SNPshotrs2066715
SNPdbers2066715
MSV3drs2066715
GWAS Ctlgrs2066715
Merged fromRs28587567
GMAF0.1281
Max Magnitude0
? (A;A) (A;G) (G;G) 28
[PMID 21247457OA-icon.png] Genetic variant of V825I in the ATP-binding cassette transporter A1 gene and serum lipid levels in the Guangxi Bai Ku Yao and Han populations

[PMID 17430597OA-icon.png] Apolipoprotein E levels in cerebrospinal fluid and the effects of ABCA1 polymorphisms.

[PMID 19041386OA-icon.png] Genetic-epidemiological evidence on genes associated with HDL cholesterol levels: a systematic in-depth review.

[PMID 19606474OA-icon.png] A survey of ABCA1 sequence variation confirms association with dementia.


GET Evidence
ABCA1-V825I
aa_change Val825Ile
aa_change_short V825I
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.0475925
summary



[PMID 23355348] Interactions of several single nucleotide polymorphisms and high body mass index on serum lipid traits.