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rs28587567

From SNPedia

Merged intors2066715
Orientationminus
Stabilizedminus
Make rs28587567(A;A)
Make rs28587567(A;G)
Make rs28587567(G;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position104825752
GeneABCA1
is asnp
is mentioned by
dbSNPrs28587567
ebirs28587567
HLIrs28587567
Exacrs28587567
Varsomers28587567
Maprs28587567
PheGenIrs28587567
hapmaprs28587567
1000 genomesrs28587567
hgdprs28587567
ensemblrs28587567
gopubmedrs28587567
geneviewrs28587567
scholarrs28587567
googlers28587567
pharmgkbrs28587567
gwascentralrs28587567
openSNPrs28587567
23andMers28587567
23andMe allrs28587567
SNP Nexus

SNPshotrs28587567
SNPdbers28587567
MSV3drs28587567
GWAS Ctlgrs28587567
StatusMerged into rs2066715
Max Magnitude
? (A;A) (A;G) (G;G) 28
Venter snp
Source plos
Gene ABCA1
allele T
frequency
sift TOLERATED
HuRef 1103652149292
Disease Association Defects in ABCA1 are a cause of high density lipoprotein deficiency type 2 (HDLD2) (MIM:604091); also known as familial hypoalphalipoproteinemia (FHA). HDLD2 is inherited as autosomal dominant trait. It is characterized by moderately low HDL cholesterol, predilection toward premature coronary artery disease (CAD) and a reduction in cellular cholesterol efflux.