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rs2167079

From SNPedia

Orientationminus
Stabilizedminus
Make rs2167079(A;A)
Make rs2167079(A;G)
Make rs2167079(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position47248704
GeneACP2, NR1H3
is asnp
is mentioned by
dbSNPrs2167079
ebirs2167079
HLIrs2167079
Exacrs2167079
Varsomers2167079
Maprs2167079
PheGenIrs2167079
hapmaprs2167079
1000 genomesrs2167079
hgdprs2167079
ensemblrs2167079
gopubmedrs2167079
geneviewrs2167079
scholarrs2167079
googlers2167079
pharmgkbrs2167079
gwascentralrs2167079
openSNPrs2167079
23andMers2167079
23andMe allrs2167079
SNP Nexus

SNPshotrs2167079
SNPdbers2167079
MSV3drs2167079
GWAS Ctlgrs2167079
GMAF0.494
Max Magnitude
? (A;A) (A;G) (G;G) 28
per the 23andMe blog, the minor allele of this SNP (T) was associated with increased HDL cholesterol
SNP Rarer allele LDL HDL TG
rs6544713 T +
rs2650000 A +
rs471364 C -
rs1800961 T -
rs7679 C - +
rs2967605 T -
rs2409722 T -
rs10903129 A - - -
rs6756629 A - + -
rs12670798 C + + +
rs7395662 A - + +
rs174570 T - - +
rs2271293 A - + -
rs2624265 C +
rs2167079 T +
rs9891572 T +
rs4844614 T +
rs5031002 G +

[PMID 17357082OA-icon.png] Identification of a novel risk locus for progressive supranuclear palsy by a pooled genomewide scan of 500,288 single-nucleotide polymorphisms.

[PMID 19060910OA-icon.png] Genome-wide association analysis of metabolic traits in a birth cohort from a founder population.


GET Evidence
ACP2-R29Q
aa_change Arg29Gln
aa_change_short R29Q
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.379657
summary